| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| TSHZ1-RNASEH2B-20-RERE | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-REOR | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-REGO | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-REGR | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-REAQ | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-ORRE | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-OROR | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-ORGO | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-ORGR | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-ORAQ | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-GORE | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-GOOR | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-GOGO | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-GOGR | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-GOAQ | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-GRRE | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-GROR | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-GRGO | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-GRGR | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-GRAQ | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-AQRE | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-AQOR | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-AQGO | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-AQGR | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-AQAQ | 20 (40 μL) | 200 μL |
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This gene encodes a colon cancer antigen that was defined by serological analysis of recombinant cDNA expression libraries. The encoded protein is a member of the teashirt C2H2-type zinc-finger protein family and may be involved in transcriptional regulation of developmental processes. Mutations in this gene may be associated with congenital aural atresia syndrome. [provided by RefSeq, Jan 2012]
Gene Symbol : TSHZ1
Gene Name : Teashirt zinc finger homeobox 1
Chromosome : CHR 18: 752,107,54-752,899,49
Locus : 18q22.3
RNase H2 is composed of a single catalytic subunit (A) and two non-catalytic subunits (B and C) and specifically degrades the RNA of RNA:DNA hybrids. The protein encoded by this gene is the non-catalytic B subunit of RNase H2, which is thought to play a role in DNA replication. Multiple transcript variants encoding different isoforms have been found for this gene. Defects in this gene are a cause of Aicardi-Goutieres syndrome type 2 (AGS2). [provided by RefSeq, Nov 2008]
Gene Symbol : RNASEH2B
Gene Name : Ribonuclease H2 subunit B
Chromosome : CHR 13: 509,096,77-509,704,61
Locus : 13q14.3
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