| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| ATP2C1-COL6A6-20-RERE | 20 (40 μL) | 200 μL |
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| ATP2C1-COL6A6-20-REOR | 20 (40 μL) | 200 μL |
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| ATP2C1-COL6A6-20-REGO | 20 (40 μL) | 200 μL |
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| ATP2C1-COL6A6-20-REGR | 20 (40 μL) | 200 μL |
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| ATP2C1-COL6A6-20-REAQ | 20 (40 μL) | 200 μL |
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| ATP2C1-COL6A6-20-ORRE | 20 (40 μL) | 200 μL |
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| ATP2C1-COL6A6-20-OROR | 20 (40 μL) | 200 μL |
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| ATP2C1-COL6A6-20-ORGO | 20 (40 μL) | 200 μL |
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| ATP2C1-COL6A6-20-ORGR | 20 (40 μL) | 200 μL |
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| ATP2C1-COL6A6-20-ORAQ | 20 (40 μL) | 200 μL |
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| ATP2C1-COL6A6-20-GORE | 20 (40 μL) | 200 μL |
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| ATP2C1-COL6A6-20-GOOR | 20 (40 μL) | 200 μL |
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| ATP2C1-COL6A6-20-GOGO | 20 (40 μL) | 200 μL |
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| ATP2C1-COL6A6-20-GOGR | 20 (40 μL) | 200 μL |
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| ATP2C1-COL6A6-20-GOAQ | 20 (40 μL) | 200 μL |
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| ATP2C1-COL6A6-20-GRRE | 20 (40 μL) | 200 μL |
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| ATP2C1-COL6A6-20-GROR | 20 (40 μL) | 200 μL |
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| ATP2C1-COL6A6-20-GRGO | 20 (40 μL) | 200 μL |
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| ATP2C1-COL6A6-20-GRGR | 20 (40 μL) | 200 μL |
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| ATP2C1-COL6A6-20-GRAQ | 20 (40 μL) | 200 μL |
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| ATP2C1-COL6A6-20-AQRE | 20 (40 μL) | 200 μL |
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| ATP2C1-COL6A6-20-AQOR | 20 (40 μL) | 200 μL |
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| ATP2C1-COL6A6-20-AQGO | 20 (40 μL) | 200 μL |
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| ATP2C1-COL6A6-20-AQGR | 20 (40 μL) | 200 μL |
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| ATP2C1-COL6A6-20-AQAQ | 20 (40 μL) | 200 μL |
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The protein encoded by this gene belongs to the family of P-type cation transport ATPases. This magnesium-dependent enzyme catalyzes the hydrolysis of ATP coupled with the transport of calcium ions. Defects in this gene cause Hailey-Hailey disease, an autosomal dominant disorder. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Aug 2011]
Gene Symbol : ATP2C1
Gene Name : ATPase secretory pathway Ca2+ transporting 1
Chromosome : CHR 3: 130,850,499-131,016,711
Locus : 3q22.1
This gene encodes a large protein that contains multiple von Willebrand factor domains and forms a component of the basal lamina of epithelial cells. This protein may regulate epithelial cell-fibronectin interactions. Variation in this gene may be implicated in skin diseases. [provided by RefSeq, May 2017]
Gene Symbol : COL6A6
Gene Name : Collagen type VI alpha 6 chain
Chromosome : CHR 3: 130,516,708-130,678,134
Locus : 3q22.1
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