| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| TRAPPC9-SLC30A8-20-RERE | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-REOR | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-REGO | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-REGR | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-REAQ | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-ORRE | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-OROR | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-ORGO | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-ORGR | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-ORAQ | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-GORE | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-GOOR | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-GOGO | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-GOGR | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-GOAQ | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-GRRE | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-GROR | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-GRGO | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-GRGR | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-GRAQ | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-AQRE | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-AQOR | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-AQGO | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-AQGR | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-AQAQ | 20 (40 μL) | 200 μL |
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This gene encodes a protein that likely plays a role in NF-kappa-B signaling. Mutations in this gene have been associated with autosomal-recessive cognitive disability. Alternatively spliced transcript variants have been described.[provided by RefSeq, Feb 2010]
Gene Symbol : TRAPPC9
Gene Name : Trafficking protein particle complex 9
Chromosome : CHR 8: 140,458,578-139,727,724
Locus : 8q24.3
The protein encoded by this gene is a zinc efflux transporter involved in the accumulation of zinc in intracellular vesicles. This gene is expressed at a high level only in the pancreas, particularly in islets of Langerhans. The encoded protein colocalizes with insulin in the secretory pathway granules of the insulin-secreting INS-1 cells. Allelic variants of this gene exist that confer susceptibility to diabetes mellitus, noninsulin-dependent (NIDDM). Several transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Mar 2010]
Gene Symbol : SLC30A8
Gene Name : Solute carrier family 30 member 8
Chromosome : CHR 8: 116,950,272-117,176,713
Locus : 8q24.11
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