| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| VPS13B-CCDC6-20-RERE | 20 (40 μL) | 200 μL |
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| VPS13B-CCDC6-20-REOR | 20 (40 μL) | 200 μL |
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| VPS13B-CCDC6-20-REGO | 20 (40 μL) | 200 μL |
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| VPS13B-CCDC6-20-REGR | 20 (40 μL) | 200 μL |
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| VPS13B-CCDC6-20-REAQ | 20 (40 μL) | 200 μL |
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| VPS13B-CCDC6-20-ORRE | 20 (40 μL) | 200 μL |
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| VPS13B-CCDC6-20-OROR | 20 (40 μL) | 200 μL |
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| VPS13B-CCDC6-20-ORGO | 20 (40 μL) | 200 μL |
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| VPS13B-CCDC6-20-ORGR | 20 (40 μL) | 200 μL |
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| VPS13B-CCDC6-20-ORAQ | 20 (40 μL) | 200 μL |
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| VPS13B-CCDC6-20-GORE | 20 (40 μL) | 200 μL |
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| VPS13B-CCDC6-20-GOOR | 20 (40 μL) | 200 μL |
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| VPS13B-CCDC6-20-GOGO | 20 (40 μL) | 200 μL |
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| VPS13B-CCDC6-20-GOGR | 20 (40 μL) | 200 μL |
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| VPS13B-CCDC6-20-GOAQ | 20 (40 μL) | 200 μL |
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| VPS13B-CCDC6-20-GRRE | 20 (40 μL) | 200 μL |
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| VPS13B-CCDC6-20-GROR | 20 (40 μL) | 200 μL |
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| VPS13B-CCDC6-20-GRGO | 20 (40 μL) | 200 μL |
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| VPS13B-CCDC6-20-GRGR | 20 (40 μL) | 200 μL |
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| VPS13B-CCDC6-20-GRAQ | 20 (40 μL) | 200 μL |
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| VPS13B-CCDC6-20-AQRE | 20 (40 μL) | 200 μL |
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| VPS13B-CCDC6-20-AQOR | 20 (40 μL) | 200 μL |
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| VPS13B-CCDC6-20-AQGO | 20 (40 μL) | 200 μL |
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| VPS13B-CCDC6-20-AQGR | 20 (40 μL) | 200 μL |
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| VPS13B-CCDC6-20-AQAQ | 20 (40 μL) | 200 μL |
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This gene encodes a coiled-coil domain-containing protein. The encoded protein is ubiquitously expressed and may function as a tumor suppressor. A chromosomal rearrangement resulting in the expression of a fusion gene containing a portion of this gene and the intracellular kinase-encoding domain of the ret proto-oncogene is the cause of thyroid papillary carcinoma.[provided by RefSeq, Sep 2010]
Gene Symbol : CCDC6
Gene Name : Coiled-coil domain containing 6
Chromosome : CHR 10: 599,066,55-597,887,46
Locus : 10q21.2
This gene encodes a potential transmembrane protein that may function in vesicle-mediated transport and sorting of proteins within the cell. This protein may play a role in the development and the function of the eye, hematological system, and central nervous system. Mutations in this gene have been associated with Cohen syndrome. Multiple splice variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]
Gene Symbol : VPS13B
Gene Name : Vacuolar protein sorting 13 homolog B
Chromosome : CHR 8: 990,070,13-998,775,85
Locus : 8q22.2
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