| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| ACTB-AHSG-20-RERE | 20 (40 μL) | 200 μL |
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| ACTB-AHSG-20-REOR | 20 (40 μL) | 200 μL |
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| ACTB-AHSG-20-REGO | 20 (40 μL) | 200 μL |
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| ACTB-AHSG-20-REGR | 20 (40 μL) | 200 μL |
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| ACTB-AHSG-20-REAQ | 20 (40 μL) | 200 μL |
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| ACTB-AHSG-20-ORRE | 20 (40 μL) | 200 μL |
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| ACTB-AHSG-20-OROR | 20 (40 μL) | 200 μL |
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| ACTB-AHSG-20-ORGO | 20 (40 μL) | 200 μL |
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| ACTB-AHSG-20-ORGR | 20 (40 μL) | 200 μL |
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| ACTB-AHSG-20-ORAQ | 20 (40 μL) | 200 μL |
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| ACTB-AHSG-20-GORE | 20 (40 μL) | 200 μL |
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| ACTB-AHSG-20-GOOR | 20 (40 μL) | 200 μL |
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| ACTB-AHSG-20-GOGO | 20 (40 μL) | 200 μL |
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| ACTB-AHSG-20-GOGR | 20 (40 μL) | 200 μL |
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| ACTB-AHSG-20-GOAQ | 20 (40 μL) | 200 μL |
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| ACTB-AHSG-20-GRRE | 20 (40 μL) | 200 μL |
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| ACTB-AHSG-20-GROR | 20 (40 μL) | 200 μL |
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| ACTB-AHSG-20-GRGO | 20 (40 μL) | 200 μL |
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| ACTB-AHSG-20-GRGR | 20 (40 μL) | 200 μL |
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| ACTB-AHSG-20-GRAQ | 20 (40 μL) | 200 μL |
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| ACTB-AHSG-20-AQRE | 20 (40 μL) | 200 μL |
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| ACTB-AHSG-20-AQOR | 20 (40 μL) | 200 μL |
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| ACTB-AHSG-20-AQGO | 20 (40 μL) | 200 μL |
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| ACTB-AHSG-20-AQGR | 20 (40 μL) | 200 μL |
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| ACTB-AHSG-20-AQAQ | 20 (40 μL) | 200 μL |
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This gene encodes one of six different actin proteins. Actins are highly conserved proteins that are involved in cell motility, structure, integrity, and intercellular signaling. The encoded protein is a major constituent of the contractile apparatus and one of the two nonmuscle cytoskeletal actins that are ubiquitously expressed. Mutations in this gene cause Baraitser-Winter syndrome 1, which is characterized by intellectual disability with a distinctive facial appearance in human patients. Numerous pseudogenes of this gene have been identified throughout the human genome. [provided by RefSeq, Aug 2017]
Gene Symbol : ACTB
Gene Name : Actin beta
Chromosome : CHR 7: 553,060,0-552,714,7
Locus : 7p22.1
The protein encoded by this gene is a negatively-charged serum glycoprotein that is synthesized by hepatocytes. The encoded protein consists of two polypeptide chains, which are both cleaved from a proprotein encoded from a single mRNA. It is involved in several processes, including endocytosis, brain development, and the formation of bone tissue. Defects in this gene are a cause of susceptibility to leanness. [provided by RefSeq, Aug 2017]
Gene Symbol : AHSG
Gene Name : Alpha 2-HS glycoprotein
Chromosome : CHR 3: 186,612,927-186,621,317
Locus : 3q27.3
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Lorem Ipsum is simply dummy text of the printing and typesetting industry.