酵母TDH1_2_3探针包括一组Quasar® 670标记的寡核苷酸以相同的比例混合在一起，终浓度是1 nmol，按照标准条件操作能够做大概80次杂交。该探针用于利用荧光原位杂交的方法检测酵母TDH1_2_3的转录本。 探针设计依据：Product was designed against glyceraldehyde-3-phosphate dehydrogenase (phosphorylating) TDH1 / TDH2 / TDH3 TDH1/2/3 a.k.a. GLD3 / GLD2 / GLD1; HSP35; HSP36; SSS2 (NCBI gene ID:853395 / 853465 / 853106) and nucleotides 1-999 of NM_001181321.3. This is an inclusive probe set design to detect the following variants: NM_001181321.3, NM_001181485.3, NM_001181666.1 该探针没有在同物种或其它物种的同源和直系同源序列上验证可能的交叉杂交。

酵母RPO21探针包括一组Quasar® 670标记的寡核苷酸以相同的比例混合在一起，终浓度是1 nmol，按照标准条件操作能够做大概80次杂交。该探针用于利用荧光原位杂交的方法检测酵母RPO21的转录本。 探针设计依据：Product was designed against DNA-directed RNA polymerase II core subunit RPO21 a.k.a. RPB1; RPB220; SUA8 (NCBI gene ID:853395) and nucleotides 1-5202 of NM_001180200.1. This is an exclusive probe set. 该探针没有在同物种或其它物种的同源和直系同源序列上验证可能的交叉杂交。

果蝇Rpll215探针包括一组Quasar® 570标记的寡核苷酸以相同的比例混合在一起，终浓度是1 nmol，按照标准条件操作能够做大概80次杂交。该探针用于利用荧光原位杂交的方法检测果蝇Rpll215的转录本。 探针设计依据：Product was designed against RNA polymerase II 215kD subunit RpII215 a.k.a. 5; 8WG16; alphaPol IIo[ser2]; CG1554; CTD; Dmel\CG1554; dRpb1; dRPB1; H5; II; IIo; l(1)10Ca; l(1)DC912; l(1)DF912; l(1)G0040; l(1)L5; L5; POL; pol II; Pol II; Pol II CTD; Pol II Ser5p; Pol II Ser5P; Pol II0[ser2]; Pol II0[ser5]; Pol IIa; Pol IIo; Pol IIo[ser2]; Pol IIo[Ser2]; Pol IIo[ser5]; Pol II[ser2]; Pol-IIa; polII; PolII; PolIIa; PolIIo; PolIIo[ser2]; PolIIo[ser5]; RNA pol II; RNA Pol II; RNA Pol II CTD; RNA pol IIo; RNA PolI 215; RNA polII; RNA PolII; RNA-PolII; RNAP; RNAP II; RNAP II LS; RNAPII; RNAPII0; RNApol; RNApol2; RNApolII; Rpb1; RPB1; RpII; rpII1; RPII215; Rpll215; Ser5-P Pol II; Ubl (NCBI gene ID:32100) and nucleotides 406-2965 of NM_078569.3. 该探针没有在同物种或其它物种的同源和直系同源序列上验证可能的交叉杂交。 Fruit Fly Rpll215 consists of a set of Quasar® 570-labeled oligos at equal ratios and pooled into a final delivered amount of 1 nmol, which yields approximately 80 hybridizations under standard conditions. Designed to detect Rpll215 transcripts in specimens using fluorescence in situ hybridization (FISH). Design Criteria: Product was designed against RNA polymerase II 215kD subunit RpII215 a.k.a. 5; 8WG16; alphaPol IIo[ser2]; CG1554; CTD; Dmel\CG1554; dRpb1; dRPB1; H5; II; IIo; l(1)10Ca; l(1)DC912; l(1)DF912; l(1)G0040; l(1)L5; L5; POL; pol II; Pol II; Pol II CTD; Pol II Ser5p; Pol II Ser5P; Pol II0[ser2]; Pol II0[ser5]; Pol IIa; Pol IIo; Pol IIo[ser2]; Pol IIo[Ser2]; Pol IIo[ser5]; Pol II[ser2]; Pol-IIa; polII; PolII; PolIIa; PolIIo; PolIIo[ser2]; PolIIo[ser5]; RNA pol II; RNA Pol II; RNA Pol II CTD; RNA pol IIo; RNA PolI 215; RNA polII; RNA PolII; RNA-PolII; RNAP; RNAP II; RNAP II LS; RNAPII; RNAPII0; RNApol; RNApol2; RNApolII; Rpb1; RPB1; RpII; rpII1; RPII215; Rpll215; Ser5-P Pol II; Ubl (NCBI gene ID:32100) and nucleotides 406-2965 of NM_078569.3. The probe set has not been tested for potential cross-hybridization to RNA(s) of paralogous and orthologous gene(s) in the same or other species. Representative image of fruit fly Rpll215 RNAs detected with a Quasar 570 dye labeled probe set in KC cells.

果蝇Rpll215探针包括一组Quasar® 670标记的寡核苷酸以相同的比例混合在一起，终浓度是1 nmol，按照标准条件操作能够做大概80次杂交。该探针用于利用荧光原位杂交的方法检测果蝇Rpll215的转录本。 探针设计依据：Product was designed against RNA polymerase II 215kD subunit RpII215 a.k.a. 5; 8WG16; alphaPol IIo[ser2]; CG1554; CTD; Dmel\CG1554; dRpb1; dRPB1; H5; II; IIo; l(1)10Ca; l(1)DC912; l(1)DF912; l(1)G0040; l(1)L5; L5; POL; pol II; Pol II; Pol II CTD; Pol II Ser5p; Pol II Ser5P; Pol II0[ser2]; Pol II0[ser5]; Pol IIa; Pol IIo; Pol IIo[ser2]; Pol IIo[Ser2]; Pol IIo[ser5]; Pol II[ser2]; Pol-IIa; polII; PolII; PolIIa; PolIIo; PolIIo[ser2]; PolIIo[ser5]; RNA pol II; RNA Pol II; RNA Pol II CTD; RNA pol IIo; RNA PolI 215; RNA polII; RNA PolII; RNA-PolII; RNAP; RNAP II; RNAP II LS; RNAPII; RNAPII0; RNApol; RNApol2; RNApolII; Rpb1; RPB1; RpII; rpII1; RPII215; Rpll215; Ser5-P Pol II; Ubl (NCBI gene ID:32100) and nucleotides 406-2965 of NM_078569.3.该探针没有在同物种或其它物种的同源和直系同源序列上验证可能的交叉杂交。 Fruit Fly Rpll215 consists of a set of Quasar® 670-labeled oligos at equal ratios and pooled into a final delivered amount of 1 nmol, which yields approximately 80 hybridizations under standard conditions. Designed to detect Rpll215 transcripts in specimens using fluorescence in situ hybridization (FISH). Design Criteria: Product was designed against RNA polymerase II 215kD subunit RpII215 a.k.a. 5; 8WG16; alphaPol IIo[ser2]; CG1554; CTD; Dmel\CG1554; dRpb1; dRPB1; H5; II; IIo; l(1)10Ca; l(1)DC912; l(1)DF912; l(1)G0040; l(1)L5; L5; POL; pol II; Pol II; Pol II CTD; Pol II Ser5p; Pol II Ser5P; Pol II0[ser2]; Pol II0[ser5]; Pol IIa; Pol IIo; Pol IIo[ser2]; Pol IIo[Ser2]; Pol IIo[ser5]; Pol II[ser2]; Pol-IIa; polII; PolII; PolIIa; PolIIo; PolIIo[ser2]; PolIIo[ser5]; RNA pol II; RNA Pol II; RNA Pol II CTD; RNA pol IIo; RNA PolI 215; RNA polII; RNA PolII; RNA-PolII; RNAP; RNAP II; RNAP II LS; RNAPII; RNAPII0; RNApol; RNApol2; RNApolII; Rpb1; RPB1; RpII; rpII1; RPII215; Rpll215; Ser5-P Pol II; Ubl (NCBI gene ID:32100) and nucleotides 406-2965 of NM_078569.3. The probe set has not been tested for potential cross-hybridization to RNA(s) of paralogous and orthologous gene(s) in the same or other species. Representative image of fruit fly Rpll215 RNAs detected with a Quasar 670 dye labeled probe set in KC cells.

果蝇Gapdh探针包括一组Quasar® 570标记的寡核苷酸以相同的比例混合在一起，终浓度是1 nmol，按照标准条件操作能够做大概80次杂交。该探针用于利用荧光原位杂交的方法检测果蝇Gapdh的转录本。 探针设计依据：Product was designed against glyceraldehyde-3-phosphate dehydrogenase Gapdh1 | 2 a.k.a. BEST:GH12586; CG12055; Dmel\CG12055; GA3PDH; GADPH; GAP; Gapd; gapdh; Gapdh; GAPDH; GAPDH I; gapdh-1; Gapdh-1; GAPDH-1; GAPDH1; Gapdh43E; GAPDHI; gh12586 | CG8893; Dmel\CG8893; GA3PDH; GADPH; GAP; Gapd; Gapdh; GAPDH; GAPDH II; Gapdh-2; Gapdh13F; GAPDH2 (NCBI gene ID:35728, 32545) and nucleotides 261-1259 of NM_080369.3. This is an inclusive probe set designed to detect the following variants: Gapdh1: NM_080369.3, NM_001038847.2, and Gapdh2: NM_080714.4, NM_001272655.1. 该探针没有在同物种或其它物种的同源和直系同源序列上验证可能的交叉杂交。 "Fruit Fly Gapdh1 | 2 consists of a set of Quasar® 570-labeled oligos at equal ratios and pooled into a final delivered amount of 1 nmol, which yields approximately 80 hybridizations under standard conditions. Designed to detect Gapdh1 | 2 transcripts in specimens using fluorescence in situ hybridization (FISH). Design Criteria: Product was designed against glyceraldehyde-3-phosphate dehydrogenase Gapdh1 | 2 a.k.a. BEST:GH12586; CG12055; Dmel\CG12055; GA3PDH; GADPH; GAP; Gapd; gapdh; Gapdh; GAPDH; GAPDH I; gapdh-1; Gapdh-1; GAPDH-1; GAPDH1; Gapdh43E; GAPDHI; gh12586 | CG8893; Dmel\CG8893; GA3PDH; GADPH; GAP; Gapd; Gapdh; GAPDH; GAPDH II; Gapdh-2; Gapdh13F; GAPDH2 (NCBI gene ID:35728, 32545) and nucleotides 261-1259 of NM_080369.3. This is an inclusive probe set designed to detect the following variants: Gapdh1: NM_080369.3, NM_001038847.2, and Gapdh2: NM_080714.4, NM_001272655.1. The probe set has not been tested for potential cross-hybridization to RNA(s) of paralogous and orthologous gene(s) in the same or other species. Representative image of fruit fly Gapdh1 | 2 RNAs detected with a Quasar 570 dye labeled probe set in KC cells."

果蝇Gapdh探针包括一组Quasar® 670标记的寡核苷酸以相同的比例混合在一起，终浓度是1 nmol，按照标准条件操作能够做大概80次杂交。该探针用于利用荧光原位杂交的方法检测果蝇Gapdh的转录本。 探针设计依据：Product was designed against glyceraldehyde-3-phosphate dehydrogenase Gapdh1 | 2 a.k.a. BEST:GH12586; CG12055; Dmel\CG12055; GA3PDH; GADPH; GAP; Gapd; gapdh; Gapdh; GAPDH; GAPDH I; gapdh-1; Gapdh-1; GAPDH-1; GAPDH1; Gapdh43E; GAPDHI; gh12586 | CG8893; Dmel\CG8893; GA3PDH; GADPH; GAP; Gapd; Gapdh; GAPDH; GAPDH II; Gapdh-2; Gapdh13F; GAPDH2 (NCBI gene ID:35728, 32545) and nucleotides 261-1259 of NM_080369.3. This is an inclusive probe set designed to detect the following variants: Gapdh1: NM_080369.3, NM_001038847.2, and Gapdh2: NM_080714.4, NM_001272655.1. 该探针没有在同物种或其它物种的同源和直系同源序列上验证可能的交叉杂交。 Fruit Fly Gapdh1 | 2 consists of a set of Quasar® 670-labeled oligos at equal ratios and pooled into a final delivered amount of 1 nmol, which yields approximately 80 hybridizations under standard conditions. Designed to detect Gapdh1 | 2 transcripts in specimens using fluorescence in situ hybridization (FISH). Design Criteria: Product was designed against glyceraldehyde-3-phosphate dehydrogenase Gapdh1 | 2 a.k.a. BEST:GH12586; CG12055; Dmel\CG12055; GA3PDH; GADPH; GAP; Gapd; gapdh; Gapdh; GAPDH; GAPDH I; gapdh-1; Gapdh-1; GAPDH-1; GAPDH1; Gapdh43E; GAPDHI; gh12586 | CG8893; Dmel\CG8893; GA3PDH; GADPH; GAP; Gapd; Gapdh; GAPDH; GAPDH II; Gapdh-2; Gapdh13F; GAPDH2 (NCBI gene ID:35728, 32545) and nucleotides 261-1259 of NM_080369.3. This is an inclusive probe set designed to detect the following variants: Gapdh1: NM_080369.3, NM_001038847.2, and Gapdh2: NM_080714.4, NM_001272655.1. The probe set has not been tested for potential cross-hybridization to RNA(s) of paralogous and orthologous gene(s) in the same or other species. Representative image of fruit fly Gapdh1 | 2 RNAs detected with a Quasar 670 dye labeled probe set in KC cells.

小鼠Polr2a探针包括一组Quasar® 570标记的寡核苷酸以相同的比例混合在一起，终浓度是1 nmol，按照标准条件操作能够做大概80次杂交。该探针用于利用荧光原位杂交的方法检测小鼠Polr2a的转录本。 探针设计依据：Product was designed against polymerase (RNA) II (DNA directed) polypeptide A Polr2a a.k.a. Rpb1; 220kDa; Rpo2-1 (NCBI gene ID:20020) and nucleotides 411-5090 of NM_001291068.1. 该探针没有在同物种或其它物种的同源和直系同源序列上验证可能的交叉杂交。

线虫AMA-1探针包括一组Quasar® 570标记的寡核苷酸以相同的比例混合在一起，终浓度是1 nmol，按照标准条件操作能够做大概80次杂交。该探针用于利用荧光原位杂交的方法检测线虫AMA-1的转录本。 探针设计依据：Product was designed against DNA-directed RNA polymerase II AMA-1 a.k.a. CELE_F36A4.7, AMA-1 (NCBI gene ID:177190) and nucleotides 51-2610 of NM_068122.6. 该探针没有在同物种或其它物种的同源和直系同源序列上验证可能的交叉杂交。

人POLR2A探针包括一组Quasar® 570标记的寡核苷酸以相同的比例混合在一起，终浓度是1 nmol，按照标准条件操作能够做大概80次杂交。该探针用于利用荧光原位杂交的方法检测人POLR2A的转录本。

探针设计依据：Product was designed against Polymerase (RNA) II (DNA directed) polypeptide A, 220kDa POLR2A a.k.a. RPB1; RPO2; POLR2; POLRA; RPOL2 (NCBI gene ID:5430) and nucleotides 387-6299 of NM_000937.4.

该探针没有在同物种或其它物种的同源和直系同源序列上验证可能的交叉杂交。

酵母RPO21探针包括一组Quasar® 570标记的寡核苷酸以相同的比例混合在一起，终浓度是1 nmol，按照标准条件操作能够做大概80次杂交。该探针用于利用荧光原位杂交的方法检测酵母RPO21的转录本。 探针设计依据：Product was designed against DNA-directed RNA polymerase II core subunit RPO21 a.k.a. RPB1; RPB220; SUA8 (NCBI gene ID:853395) and nucleotides 1-5202 of NM_001180200.1. This is an exclusive probe set. 该探针没有在同物种或其它物种的同源和直系同源序列上验证可能的交叉杂交。

人TFRC探针包括一组Quasar® 570标记的寡核苷酸以相同的比例混合在一起，终浓度是1 nmol，按照标准条件操作能够做大概80次杂交。该探针用于利用荧光原位杂交的方法检测人TFRC的转录本。 探针设计依据：人铁传递蛋白受体1（Human Transferrin receptor 1, TFRC）, 又名 T9; TR; TFR; p90; CD71; TFR1; TRFR (NCBI gene ID: 7037), 针对编码序列 NM_003234.2 nts 284-2566设计探针，该探针组也可以用来检测以下转录本变体： NM_001128148。 该探针没有在同物种或其它物种的同源和直系同源序列上验证可能的交叉杂交。 Human TFRC consists of a set of Quasar® 570-labeled oligos mixed at equal ratios and pooled into a final delivered amount of 1 nmol, which yields approximately 80 hybridizations under standard conditions. Designed to detect TFRC transcripts in Human specimens using fluorescence in situ hybridization (FISH). Design Criteria: Product was designed against Human Transferrin receptor 1, TFRC, a.k.a. T9; TR; TFR; p90; CD71; TFR1; TRFR (NCBI gene ID: 7037), and the coding sequence of NM_003234.2 nts 284-2566.This is an inclusive probe set designed to also detect the following variant: NM_001128148.The probe set has not been tested for potential cross-hybridzation to RNA(s) of paralogous and orthologous gene(s) in the same or other species. Representative image of human TFRC mRNAs detected with a Quasar 570 dye labeled probe set in A549 cells。

人GAPDH探针包括一组Quasar® 570标记的寡核苷酸以相同的比例混合在一起，终浓度是1 nmol，按照标准条件操作能够做大概80次杂交。该探针用于利用荧光原位杂交的方法检测人GAPDH的转录本。 探针设计依据：Product was designed against Human Glyceraldehyde-3-phosphate dehydrogenase, GAPDH, a.k.a. G3PD; GAPD (NCBI gene ID: 2597), and the coding sequence of NM_002046.4 nts 175-1182. 该探针没有在同物种或其它物种的同源和直系同源序列上验证可能的交叉杂交。 Human GAPDH consists of a set of Quasar® 570-labeled oligos mixed at equal ratios and pooled into a final delivered amount of 1 nmol, which yields approximately 80 hybridizations under standard conditions. Designed to detect GAPDH transcripts in Human specimens using fluorescence in situ hybridization (FISH). Design Criteria: Product was designed against Human Glyceraldehyde-3-phosphate dehydrogenase, GAPDH, a.k.a. G3PD; GAPD (NCBI gene ID: 2597), and the coding sequence of NM_002046.4 nts 175-1182.The probe set has not been tested for potential cross-hybridization to RNA(s) of paralogous and orthologous gene(s) in the same or other species. Representative image of human GAPDH mRNAs detected with a Quasar 570 dye labeled probe set in A549 cells.

人GAPDH探针包括一组Quasar® 670标记的寡核苷酸以相同的比例混合在一起，终浓度是1 nmol，按照标准条件操作能够做大概80次杂交。该探针用于利用荧光原位杂交的方法检测人GAPDH的转录本。 探针设计依据：Product was designed against Human Glyceraldehyde-3-phosphate dehydrogenase, GAPDH, a.k.a. G3PD; GAPD (NCBI gene ID: 2597), and the coding sequence of NM_002046.4 nts 175-1182. 该探针没有在同物种或其它物种的同源和直系同源序列上验证可能的交叉杂交。 Human GAPDH consists of a set of Quasar® 670-labeled oligos mixed at equal ratios and pooled into a final delivered amount of 1 nmol, which yields approximately 80 hybridizations under standard conditions. Designed to detect GAPDH transcripts in Human specimens using fluorescence in situ hybridization (FISH). Design Criteria: Product was designed against Human Glyceraldehyde-3-phosphate dehydrogenase, GAPDH, a.k.a. G3PD; GAPD (NCBI gene ID: 2597), and the coding sequence of NM_002046.4 nts 175-1182.The probe set has not been tested for potential cross-hybridization to RNA(s) of paralogous and orthologous gene(s) in the same or other species. Representative image of human GAPDH mRNAs detected with a Quasar 570 dye labeled probe set in A549 cells.

人MALAT1探针包括一组Quasar® 570标记的寡核苷酸以相同的比例混合在一起，终浓度是1 nmol，按照标准条件操作能够做大概80次杂交。该探针用于利用荧光原位杂交的方法检测人MALAT1的转录本。 探针设计依据：Product was designed against Human metastasis associated lung adenocarcinoma transcript 1 (non-protein coding), MALAT1, a.k.a. HCN; NEAT2; MALAT-1; PRO2853; LINC00047; NCRNA00047 (NCBI gene ID: 378938), and the mature sequence of NR_002819.2 nts1284-8355. 该探针没有在同物种或其它物种的同源和直系同源序列上验证可能的交叉杂交。 Human MALAT1 consists of a set of Quasar® 570-labeled oligos mixed at equal ratios and pooled into a final delivered amount of 1 nmol, which yields approximately 80 hybridizations under standard conditions. Designed to detect MALAT1 transcripts in Human specimens using fluorescence in situ hybridization (FISH). Design Criteria: Product was designed against Human metastasis associated lung adenocarcinoma transcript 1 (non-protein coding), MALAT1, a.k.a. HCN; NEAT2; MALAT-1; PRO2853; LINC00047; NCRNA00047 (NCBI gene ID: 378938), and the mature sequence of NR_002819.2 nts1284-8355.The probe set has not been tested for potential cross-hybridization to RNA(s) of paralogous and orthologous gene(s) in the same or other species. Representative image of human MALAT1 RNAs detected with a Quasar 570 dye labeled probe set in A549 cells.

人MALAT1探针包括一组Quasar® 670标记的寡核苷酸以相同的比例混合在一起，终浓度是1 nmol，按照标准条件操作能够做大概80次杂交。该探针用于利用荧光原位杂交的方法检测人MALAT1的转录本。 探针设计依据：Product was designed against Human metastasis associated lung adenocarcinoma transcript 1 (non-protein coding), MALAT1, a.k.a. HCN; NEAT2; MALAT-1; PRO2853; LINC00047; NCRNA00047 (NCBI gene ID: 378938), and the mature sequence of NR_002819.2 nts1284-8355. 该探针没有在同物种或其它物种的同源和直系同源序列上验证可能的交叉杂交。

小鼠Gapdh探针包括一组Quasar® 570标记的寡核苷酸以相同的比例混合在一起，终浓度是1 nmol，按照标准条件操作能够做大概80次杂交。该探针用于利用荧光原位杂交的方法检测小鼠Gapdh的转录本。 探针设计依据：小鼠甘油醛-3-磷酸脱氢酶（Mouse glyceraldehyde-3-phosphate dehydrogenase, Gapdh）, 又名G3PD、Gapd (NCBI gene ID: 14433), 针对编码序列NM_008084.2 第51-1052段序列设计。 该探针没有在同物种或其它物种的同源和直系同源序列上验证可能的交叉杂交。

人NEAT1 5' Segment探针包括一组Quasar® 570标记的寡核苷酸以相同的比例混合在一起，终浓度是1 nmol，按照标准条件操作能够做大概80次杂交。该探针用于利用荧光原位杂交的方法检测人NEAT1 5' Segment的转录本。 探针设计依据：Product was designed against Human nuclear paraspeckle assembly transcript 1 (non-protein coding), NEAT1_5, a.k.a. TncRNA; LINC00084; NCRNA00084 (NCBI gene ID: 283131), and the short and long variant of NR_028272.1 nts 1-3756.This is an inclusive probe set designed to also detect the following variant: GQ859162. 该探针没有在同物种或其它物种的同源和直系同源序列上验证可能的交叉杂交。 Human NEAT1_5 consists of a set of Quasar® 570-labeled oligos mixed at equal ratios and pooled into a final delivered amount of 1 nmol, which yields approximately 80 hybridizations under standard conditions. Designed to detect NEAT1_5 transcripts in Human specimens using fluorescence in situ hybridization (FISH). Design Criteria: Product was designed against Human nuclear paraspeckle assembly transcript 1 (non-protein coding), NEAT1_5, a.k.a. TncRNA; LINC00084; NCRNA00084 (NCBI gene ID: 283131), and the short and long variant of NR_028272.1 nts 1-3756.This is an inclusive probe set designed to also detect the following variant: GQ859162. The probe set has not been tested for potential cross-hybridization to RNA(s) of paralogous and orthologous gene(s) in the same or other species. Representative image of human NEAT1_5 RNAs detected with a Quasar 570 dye labeled probe set in A549 cells.

人NEAT2 Middle Segment探针包括一组Quasar® 570标记的寡核苷酸以相同的比例混合在一起，终浓度是1 nmol，按照标准条件操作能够做大概80次杂交。该探针用于利用荧光原位杂交的方法检测人NEAT2 Middle Segment的转录本。 探针设计依据：Product was designed against Human nuclear paraspeckle assembly transcript 1 (non-protein coding), NEAT1_m, a.k.a. TncRNA; LINC00084; NCRNA00084 (NCBI gene ID: 283131), and the middle segment of the long variant of NR_028272.1 nts 3800-11700. 该探针没有在同物种或其它物种的同源和直系同源序列上验证可能的交叉杂交。 Human NEAT1_m consists of a set of Quasar® 570-labeled oligos mixed at equal ratios and pooled into a final delivered amount of 1 nmol, which yields approximately 80 hybridizations under standard conditions. Designed to detect NEAT1_m transcripts in Human specimens using fluorescence in situ hybridization (FISH). Design Criteria: Product was designed against Human nuclear paraspeckle assembly transcript 1 (non-protein coding), NEAT1_m, a.k.a. TncRNA; LINC00084; NCRNA00084 (NCBI gene ID: 283131), and the middle segment of the long variant of NR_028272.1 nts 3800-11700.The probe set has not been tested for potential cross-hybridization to RNA(s) of paralogous and orthologous gene(s) in the same or other species. Representative image of human NEAT1_m RNAs detected with a Quasar 570 dye labeled probe set in A549 cells.

人XIST探针包括一组Quasar® 570标记的寡核苷酸以相同的比例混合在一起，终浓度是1 nmol，按照标准条件操作能够做大概80次杂交。该探针用于利用荧光原位杂交的方法检测人XIST的转录本。 探针设计依据：Product was designed against Human X (inactive)-specific transcript (non-protein coding), XIST, a.k.a. XCE; XIC; SXI1; swd66; DXS1089; DXS399E; LINC00001; NCRNA00001 (NCBI gene ID: 7503), and the sequence of NR_001564.2 nts 1-8000. 该探针没有在同物种或其它物种的同源和直系同源序列上验证可能的交叉杂交。 Human XIST consists of a set of Quasar® 570-labeled oligos mixed at equal ratios and pooled into a final delivered amount of 1 nmol, which yields approximately 80 hybridizations under standard conditions. Designed to detect XIST transcripts in Human specimens using fluorescence in situ hybridization (FISH). Design Criteria: Product was designed against Human X (inactive)-specific transcript (non-protein coding), XIST, a.k.a. XCE; XIC; SXI1; swd66; DXS1089; DXS399E; LINC00001; NCRNA00001 (NCBI gene ID: 7503), and the sequence of NR_001564.2 nts 1-8000.The probe set has not been tested for potential cross-hybridization to RNA(s) of paralogous and orthologous gene(s) in the same or other species. Representative image of human XIST mRNAs detected with a Quasar 570 dye labeled probe set in MCF7 cells.

小鼠Gapdh探针包括一组Quasar® 670标记的寡核苷酸以相同的比例混合在一起，终浓度是1 nmol，按照标准条件操作能够做大概80次杂交。该探针用于利用荧光原位杂交的方法检测小鼠Gapdh的转录本。 探针设计依据：小鼠甘油醛-3-磷酸脱氢酶（Mouse glyceraldehyde-3-phosphate dehydrogenase, Gapdh）, 又名G3PD、Gapd (NCBI gene ID: 14433), 针对编码序列NM_008084.2 第51-1052段序列设计。 该探针没有在同物种或其它物种的同源和直系同源序列上验证可能的交叉杂交。用Quasar 670染料标记的探针组检测小鼠Gapdh mRNAs的代表图片是在NIH 3T3细胞上完成的。 Mouse Gapdh consists of a set of Quasar® 670-labeled oligos mixed at equal ratios and pooled into a final delivered amount of 1 nmol, which yields approximately 80 hybridizations under standard conditions. Designed to detect Gapdh transcripts in Mouse specimens using fluorescence in situ hybridization (FISH). Design Criteria: Product was designed against Mouse glyceraldehyde-3-phosphate dehydrogenase, Gapdh, a.k.a. G3PD; Gapd; (NCBI gene ID: 14433), and the coding sequence of NM_008084.2 nts 51-1052.The probe set has not been tested for potential cross-hybridization to RNA(s) of paralogous and orthologous gene(s) in the same or other species. Representative image of mouse Gapdh mRNAs detected with a Quasar 670 dye labeled probe set in NIH 3T3 cells.

小鼠Tfrc探针包括一组Quasar® 570标记的寡核苷酸以相同的比例混合在一起，终浓度是1 nmol，按照标准条件操作能够做大概80次杂交。该探针用于利用荧光原位杂交的方法检测小鼠Tfrc的转录本。 探针设计依据：Product was designed against Mouse transferrin receptor, Tfrc, a.k.a. TR; TFR; p90; CD71; TFR1; Trfr; Mtvr1; Mtvr-1; AI195355; AI426448; AU015758; 2610028K12Rik; E430033M20Rik (NCBI gene ID: 22042), and the coding sequence of NM_011638.4 nts 165-2456. 该探针没有在同物种或其它物种的同源和直系同源序列上验证可能的交叉杂交。 Mouse Tfrc consists of a set of Quasar® 570-labeled oligos mixed at equal ratios and pooled into a final delivered amount of 1 nmol, which yields approximately 80 hybridizations under standard conditions. Designed to detect Tfrc transcripts in Mouse specimens using fluorescence in situ hybridization (FISH). Design Criteria: Product was designed against Mouse transferrin receptor, Tfrc, a.k.a. TR; TFR; p90; CD71; TFR1; Trfr; Mtvr1; Mtvr-1; AI195355; AI426448; AU015758; 2610028K12Rik; E430033M20Rik (NCBI gene ID: 22042), and the coding sequence of NM_011638.4 nts 165-2456.The probe set has not been tested for potential cross-hybridization to RNA(s) of paralogous and orthologous gene(s) in the same or other species. Representative image of mouse Tfrc mRNAs detected with a Quasar 570 dye labeled probe set in NIH 3T3 cells.

小鼠Malat1探针包括一组Quasar® 570标记的寡核苷酸以相同的比例混合在一起，终浓度是1 nmol，按照标准条件操作能够做大概80次杂交。该探针用于利用荧光原位杂交的方法检测小鼠Malat1的转录本。 探针设计依据：Product was designed against Mouse metastasis associated lung adenocarcinoma transcript 1 (non-coding RNA), Malat1, a.k.a. NEAT2; AI647968; 2210401K01Rik; 9430072K23Rik (NCBI gene ID: 72289), and the sequence of NR_002847.2 nts 751-6982. 该探针没有在同物种或其它物种的同源和直系同源序列上验证可能的交叉杂交。 Mouse Malat1 consists of a set of Quasar® 570-labeled oligos mixed at equal ratios and pooled into a final delivered amount of 1 nmol, which yields approximately 80 hybridizations under standard conditions. Designed to detect Malat1 transcripts in Mouse specimens using fluorescence in situ hybridization (FISH). Design Criteria: Product was designed against Mouse metastasis associated lung adenocarcinoma transcript 1 (non-coding RNA), Malat1, a.k.a. NEAT2; AI647968; 2210401K01Rik; 9430072K23Rik (NCBI gene ID: 72289), and the sequence of NR_002847.2 nts 751-6982.The probe set has not been tested for potential cross-hybridization to RNA(s) of paralogous and orthologous gene(s) in the same or other species. Representative image of mouse Malat1 RNAs detected with a Quasar 570 dye labeled probe set in NIH-3T3 cells.

小鼠Neat1 5' Segment探针包括一组Quasar® 570标记的寡核苷酸以相同的比例混合在一起，终浓度是1 nmol，按照标准条件操作能够做大概80次杂交。该探针用于利用荧光原位杂交的方法检测小鼠Neat1 5' Segment的转录本。 探针设计依据：Product was designed against Mouse nuclear paraspeckle assembly transcript 1 (non-protein coding), Neat1_5, a.k.a.VINC; 2310043N10Rik (NCBI gene ID: 66961), and the short and long variant of NR_003513.2 nts 1-3177.This is an inclusive probe set designed to detect also the following RNA(s): GQ859163 nts 1-3756. 该探针没有在同物种或其它物种的同源和直系同源序列上验证可能的交叉杂交。 Mouse Neat1_5 consists of a set of Quasar® 570-labeled oligos mixed at equal ratios and pooled into a final delivered amount of 1 nmol, which yields approximately 80 hybridizations under standard conditions. Designed to detect Neat1_5 transcripts in Mouse specimens using fluorescence in situ hybridization (FISH). Design Criteria: Product was designed against Mouse nuclear paraspeckle assembly transcript 1 (non-protein coding), Neat1_5, a.k.a.VINC; 2310043N10Rik (NCBI gene ID: 66961), and the short and long variant of NR_003513.2 nts 1-3177.This is an inclusive probe set designed to detect also the following RNA(s): GQ859163 nts 1-3756. The probe set has not been tested for potential cross-hybridization to RNA(s) of paralogous and orthologous gene(s) in the same or other species. Representative image of mouse Neat1_5 RNAs detected with a Quasar 570 dye labeled probe set in NIH-3T3 cells.

小鼠Neat1 Middle Segment探针包括一组Quasar® 570标记的寡核苷酸以相同的比例混合在一起，终浓度是1 nmol，按照标准条件操作能够做大概80次杂交。该探针用于利用荧光原位杂交的方法检测小鼠Neat1 Middle Segment的转录本。 探针设计依据：Product was designed against Mouse nuclear paraspeckle assembly transcript 1 (non-protein coding), Neat1_m, a.k.a. VINC; 2310043N10Rik (NCBI gene ID: 66961), and the middle of the long variant of GQ859163 nts 4001-12000. 该探针没有在同物种或其它物种的同源和直系同源序列上验证可能的交叉杂交。 Mouse Neat1_m consists of a set of Quasar® 570-labeled oligos mixed at equal ratios and pooled into a final delivered amount of 1 nmol, which yields approximately 80 hybridizations under standard conditions. Designed to detect Neat1_m transcripts in Mouse specimens using fluorescence in situ hybridization (FISH). Design Criteria: Product was designed against Mouse nuclear paraspeckle assembly transcript 1 (non-protein coding), Neat1_m, a.k.a. VINC; 2310043N10Rik (NCBI gene ID: 66961), and the middle of the long variant of GQ859163 nts 4001-12000.The probe set has not been tested for potential cross-hybridization to RNA(s) of paralogous and orthologous gene(s) in the same or other species. Representative image of mouse Neat1_m RNAs detected with a Quasar 570 dye labeled probe set in NIH 3T3 cells.

小鼠Xist探针包括一组Quasar® 570标记的寡核苷酸以相同的比例混合在一起，终浓度是1 nmol，按照标准条件操作能够做大概80次杂交。该探针用于利用荧光原位杂交的方法检测小鼠Xist的转录本。 探针设计依据：Product was designed against Mouse X inactive specific transcripts (non-protein coding), Xist, a.k.a. AI314753; A430022B1 (NCBI gene ID: 213742), and the sequence of NR_001570.2 nts 1-8000. 该探针没有在同物种或其它物种的同源和直系同源序列上验证可能的交叉杂交。 Mouse Xist consists of a set of Quasar® 570-labeled oligos mixed at equal ratios and pooled into a final delivered amount of 1 nmol, which yields approximately 80 hybridizations under standard conditions. Designed to detect Xist transcripts in Mouse specimens using fluorescence in situ hybridization (FISH). Design Criteria: Product was designed against Mouse X inactive specific transcripts (non-protein coding), Xist, a.k.a. AI314753; A430022B1 (NCBI gene ID: 213742), and the sequence of NR_001570.2 nts 1-8000.The probe set has not been tested for potential cross-hybridization to RNA(s) of paralogous and orthologous gene(s) in the same or other species. Representative image of mouse Xist RNAs detected with a Quasar 570 dye labeled probe set in Neuro-2a cells.

酵母TDH1_2_3探针包括一组Quasar® 570标记的寡核苷酸以相同的比例混合在一起，终浓度是1 nmol，按照标准条件操作能够做大概80次杂交。该探针用于利用荧光原位杂交的方法检测酵母TDH1_2_3的转录本。 探针设计依据：Product was designed against glyceraldehyde-3-phosphate dehydrogenase (phosphorylating) TDH1 / TDH2 / TDH3 TDH1/2/3 a.k.a. GLD3 / GLD2 / GLD1; HSP35; HSP36; SSS2 (NCBI gene ID:853395 / 853465 / 853106) and nucleotides 1-999 of NM_001181321.3. This is an inclusive probe set design to detect the following variants: NM_001181321.3, NM_001181485.3, NM_001181666.1 该探针没有在同物种或其它物种的同源和直系同源序列上验证可能的交叉杂交。

设计您自己的自定义Stellaris®RNA FISH探针来检测你感兴趣的RNA。通过使用LGC Biosearch在线Stellaris RNA FISH探针设计工具Stellaris RNA FISH probe designer，可以设计得到多达48个荧光单独标记的寡核苷酸来结合并可视化待检测的靶标RNA。在开始您的Stellaris RNA FISH自定义探针设计之前，可以通过在DesignReady探针界面的搜索框内输入感兴趣的RNA名称来确认LGC Biosearch是否已经有针对您需要检测的靶标有设计好的探针。LGC Biosearch还提供Stellaris ShipReady探针可作为您实验的阳性对照，以及Stellaris缓冲液，作为探针的好搭配，能够让RNA的检测与分析更强大。 产品形式：一组Stellaris FISH探针集包含荧光标记的高达48种寡核苷酸的混合物，提供冻干粉形式。 交付量：5 nmol汇集的寡核苷酸（根据每种靶标更优的稀释度可以做200-400次杂交实验）。 价格：所有自定义FISH探针价格统一。 设计周期：5-7个工作日。 Design your own Custom Stellaris® RNA FISH Probe Set to detect your RNA of interest. By using our Stellaris RNA FISH probe designer, you can design up to 48 individually fluorescently labeled oligonucleotides to bind along and visualize your target RNA. Before you begin designing your Stellaris RNA FISH probe set, check to see if we have already designed a set against your target of interest by entering your target into the search box on our DesignReady page. We also offer Stellaris ShipReady probe sets to be used as controls for your experiment and Stellaris Buffers, which are the perfect accompaniment to your probe sets, allowing for even more robust RNA detection and analysis. Product information: One set of Stellaris FISH probes contain a blend of up to 48 oligos labeled with a fluorophore. Probes arrive lyophilized and ready to use. Delivered Amount: 5 nmol of pooled oligos (200-400 hybridization experiments depending on optimal working dilutions for each target). Price: Same price for all custom Stellaris probes. Turnaround time: 5 to 7 business days.

设计您自己的自定义Stellaris®RNA FISH探针来检测你感兴趣的RNA。通过使用LGC Biosearch在线Stellaris RNA FISH探针设计工具Stellaris RNA FISH probe designer，可以设计得到多达48个荧光单独标记的寡核苷酸来结合并可视化待检测的靶标RNA。在开始您的Stellaris RNA FISH自定义探针设计之前，可以通过在DesignReady探针界面的搜索框内输入感兴趣的RNA名称来确认LGC Biosearch是否已经有针对您需要检测的靶标有设计好的探针。LGC Biosearch还提供Stellaris ShipReady探针可作为您实验的阳性对照，以及Stellaris缓冲液，作为探针的好搭配，能够让RNA的检测与分析更强大。 产品形式：一组Stellaris FISH探针集包含荧光标记的高达48种寡核苷酸的混合物，提供冻干粉形式。 交付量：5 nmol汇集的寡核苷酸（根据每种靶标更优的稀释度可以做200-400次杂交实验）。 价格：所有自定义FISH探针价格统一。 设计周期：5-7个工作日。 Design your own Custom Stellaris® RNA FISH Probe Set to detect your RNA of interest. By using our Stellaris RNA FISH probe designer, you can design up to 48 individually fluorescently labeled oligonucleotides to bind along and visualize your target RNA. Before you begin designing your Stellaris RNA FISH probe set, check to see if we have already designed a set against your target of interest by entering your target into the search box on our DesignReady page. We also offer Stellaris ShipReady probe sets to be used as controls for your experiment and Stellaris Buffers, which are the perfect accompaniment to your probe sets, allowing for even more robust RNA detection and analysis. Product information: One set of Stellaris FISH probes contain a blend of up to 48 oligos labeled with a fluorophore. Probes arrive lyophilized and ready to use. Delivered Amount: 5 nmol of pooled oligos (200-400 hybridization experiments depending on optimal working dilutions for each target). Price: Same price for all custom Stellaris probes. Turnaround time: 5 to 7 business days.

设计您自己的自定义Stellaris®RNA FISH探针来检测你感兴趣的RNA。通过使用LGC Biosearch在线Stellaris RNA FISH探针设计工具Stellaris RNA FISH probe designer，可以设计得到多达48个荧光单独标记的寡核苷酸来结合并可视化待检测的靶标RNA。在开始您的Stellaris RNA FISH自定义探针设计之前，可以通过在DesignReady探针界面的搜索框内输入感兴趣的RNA名称来确认LGC Biosearch是否已经有针对您需要检测的靶标有设计好的探针。LGC Biosearch还提供Stellaris ShipReady探针可作为您实验的阳性对照，以及Stellaris缓冲液，作为探针的好搭配，能够让RNA的检测与分析更强大。 产品形式：一组Stellaris FISH探针集包含荧光标记的高达48种寡核苷酸的混合物，提供冻干粉形式。 交付量：5 nmol汇集的寡核苷酸（根据每种靶标更优的稀释度可以做200-400次杂交实验）。 价格：所有自定义FISH探针价格统一。 设计周期：5-7个工作日。 Design your own Custom Stellaris® RNA FISH Probe Set to detect your RNA of interest. By using our Stellaris RNA FISH probe designer, you can design up to 48 individually fluorescently labeled oligonucleotides to bind along and visualize your target RNA. Before you begin designing your Stellaris RNA FISH probe set, check to see if we have already designed a set against your target of interest by entering your target into the search box on our DesignReady page. We also offer Stellaris ShipReady probe sets to be used as controls for your experiment and Stellaris Buffers, which are the perfect accompaniment to your probe sets, allowing for even more robust RNA detection and analysis. Product information: One set of Stellaris FISH probes contain a blend of up to 48 oligos labeled with a fluorophore. Probes arrive lyophilized and ready to use. Delivered Amount: 5 nmol of pooled oligos (200-400 hybridization experiments depending on optimal working dilutions for each target). Price: Same price for all custom Stellaris probes. Turnaround time: 5 to 7 business days.

设计您自己的自定义Stellaris®RNA FISH探针来检测你感兴趣的RNA。通过使用LGC Biosearch在线Stellaris RNA FISH探针设计工具Stellaris RNA FISH probe designer，可以设计得到多达48个荧光单独标记的寡核苷酸来结合并可视化待检测的靶标RNA。在开始您的Stellaris RNA FISH自定义探针设计之前，可以通过在DesignReady探针界面的搜索框内输入感兴趣的RNA名称来确认LGC Biosearch是否已经有针对您需要检测的靶标有设计好的探针。LGC Biosearch还提供Stellaris ShipReady探针可作为您实验的阳性对照，以及Stellaris缓冲液，作为探针的好搭配，能够让RNA的检测与分析更强大。 产品形式：一组Stellaris FISH探针集包含荧光标记的高达48种寡核苷酸的混合物，提供冻干粉形式。 交付量：5 nmol汇集的寡核苷酸（根据每种靶标更优的稀释度可以做200-400次杂交实验）。 价格：所有自定义FISH探针价格统一。 设计周期：5-7个工作日。 Design your own Custom Stellaris® RNA FISH Probe Set to detect your RNA of interest. By using our Stellaris RNA FISH probe designer, you can design up to 48 individually fluorescently labeled oligonucleotides to bind along and visualize your target RNA. Before you begin designing your Stellaris RNA FISH probe set, check to see if we have already designed a set against your target of interest by entering your target into the search box on our DesignReady page. We also offer Stellaris ShipReady probe sets to be used as controls for your experiment and Stellaris Buffers, which are the perfect accompaniment to your probe sets, allowing for even more robust RNA detection and analysis. Product information: One set of Stellaris FISH probes contain a blend of up to 48 oligos labeled with a fluorophore. Probes arrive lyophilized and ready to use. Delivered Amount: 5 nmol of pooled oligos (200-400 hybridization experiments depending on optimal working dilutions for each target). Price: Same price for all custom Stellaris probes. Turnaround time: 5 to 7 business days.