| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| ANO6-EDA-20-RERE | 20 (40 μL) | 200 μL |
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| ANO6-EDA-20-REOR | 20 (40 μL) | 200 μL |
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| ANO6-EDA-20-REGO | 20 (40 μL) | 200 μL |
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| ANO6-EDA-20-REGR | 20 (40 μL) | 200 μL |
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| ANO6-EDA-20-REAQ | 20 (40 μL) | 200 μL |
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| ANO6-EDA-20-ORRE | 20 (40 μL) | 200 μL |
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| ANO6-EDA-20-OROR | 20 (40 μL) | 200 μL |
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| ANO6-EDA-20-ORGO | 20 (40 μL) | 200 μL |
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| ANO6-EDA-20-ORGR | 20 (40 μL) | 200 μL |
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| ANO6-EDA-20-ORAQ | 20 (40 μL) | 200 μL |
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| ANO6-EDA-20-GORE | 20 (40 μL) | 200 μL |
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| ANO6-EDA-20-GOOR | 20 (40 μL) | 200 μL |
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| ANO6-EDA-20-GOGO | 20 (40 μL) | 200 μL |
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| ANO6-EDA-20-GOGR | 20 (40 μL) | 200 μL |
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| ANO6-EDA-20-GOAQ | 20 (40 μL) | 200 μL |
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| ANO6-EDA-20-GRRE | 20 (40 μL) | 200 μL |
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| ANO6-EDA-20-GROR | 20 (40 μL) | 200 μL |
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| ANO6-EDA-20-GRGO | 20 (40 μL) | 200 μL |
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| ANO6-EDA-20-GRGR | 20 (40 μL) | 200 μL |
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| ANO6-EDA-20-GRAQ | 20 (40 μL) | 200 μL |
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| ANO6-EDA-20-AQRE | 20 (40 μL) | 200 μL |
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| ANO6-EDA-20-AQOR | 20 (40 μL) | 200 μL |
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| ANO6-EDA-20-AQGO | 20 (40 μL) | 200 μL |
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| ANO6-EDA-20-AQGR | 20 (40 μL) | 200 μL |
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| ANO6-EDA-20-AQAQ | 20 (40 μL) | 200 μL |
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The protein encoded by this gene is a type II membrane protein that can be cleaved by furin to produce a secreted form. The encoded protein, which belongs to the tumor necrosis factor family, acts as a homotrimer and may be involved in cell-cell signaling during the development of ectodermal organs. Defects in this gene are a cause of ectodermal dysplasia, anhidrotic, which is also known as X-linked hypohidrotic ectodermal dysplasia. Several transcript variants encoding many different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Gene Symbol : EDA
Gene Name : Ectodysplasin A
Chromosome : CHR X: 696,160,66-700,394,71
Locus : Xq13.1
This gene encodes a multi-pass transmembrane protein that belongs to the anoctamin family. This protein is an essential component for the calcium-dependent exposure of phosphatidylserine on the cell surface. The scrambling of phospholipid occurs in various biological systems, such as when blood platelets are activated, they expose phosphatidylserine to trigger the clotting system. Mutations in this gene are associated with Scott syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Mar 2011]
Gene Symbol : ANO6
Gene Name : Anoctamin 6
Chromosome : CHR 12: 452,159,86-454,404,03
Locus : 12q12
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