| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| ACTB-KIAA0182-20-RERE | 20 (40 μL) | 200 μL |
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| ACTB-KIAA0182-20-REOR | 20 (40 μL) | 200 μL |
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| ACTB-KIAA0182-20-REGO | 20 (40 μL) | 200 μL |
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| ACTB-KIAA0182-20-REGR | 20 (40 μL) | 200 μL |
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| ACTB-KIAA0182-20-REAQ | 20 (40 μL) | 200 μL |
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| ACTB-KIAA0182-20-ORRE | 20 (40 μL) | 200 μL |
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| ACTB-KIAA0182-20-OROR | 20 (40 μL) | 200 μL |
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| ACTB-KIAA0182-20-ORGO | 20 (40 μL) | 200 μL |
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| ACTB-KIAA0182-20-ORGR | 20 (40 μL) | 200 μL |
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| ACTB-KIAA0182-20-ORAQ | 20 (40 μL) | 200 μL |
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| ACTB-KIAA0182-20-GORE | 20 (40 μL) | 200 μL |
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| ACTB-KIAA0182-20-GOOR | 20 (40 μL) | 200 μL |
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| ACTB-KIAA0182-20-GOGO | 20 (40 μL) | 200 μL |
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| ACTB-KIAA0182-20-GOGR | 20 (40 μL) | 200 μL |
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| ACTB-KIAA0182-20-GOAQ | 20 (40 μL) | 200 μL |
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| ACTB-KIAA0182-20-GRRE | 20 (40 μL) | 200 μL |
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| ACTB-KIAA0182-20-GROR | 20 (40 μL) | 200 μL |
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| ACTB-KIAA0182-20-GRGO | 20 (40 μL) | 200 μL |
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| ACTB-KIAA0182-20-GRGR | 20 (40 μL) | 200 μL |
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| ACTB-KIAA0182-20-GRAQ | 20 (40 μL) | 200 μL |
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| ACTB-KIAA0182-20-AQRE | 20 (40 μL) | 200 μL |
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| ACTB-KIAA0182-20-AQOR | 20 (40 μL) | 200 μL |
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| ACTB-KIAA0182-20-AQGO | 20 (40 μL) | 200 μL |
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| ACTB-KIAA0182-20-AQGR | 20 (40 μL) | 200 μL |
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| ACTB-KIAA0182-20-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
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