SLC10A2 FISH Probe
The SLC10A2 FISH probe is designed to hybridize to the SLC10A2 gene and is primarily used for detecting amplifications and deletions associated with the gene. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe can be labeled in one of five colors. Each probe is sold in a 20 test kit (approximately 20 slides - 22x22 mm area) and includes hybridization buffer. Please note that due to design optimizations, prices are subject to change.
** This product is for in vitro and research use only. This product is not intended for diagnostic use.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SLC10A2-20-OR (Standard Design) | 20 (40 μL) | 200 μL |  |
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| SLC10A2-20-RE | 20 (40 μL) | 200 μL |  |
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| SLC10A2-20-GO | 20 (40 μL) | 200 μL |  |
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| SLC10A2-20-GR | 20 (40 μL) | 200 μL |  |
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| SLC10A2-20-AQ | 20 (40 μL) | 200 μL |  |
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| SLC10A2-20-DIG | 20 (40 μL) | 200 μL |  |
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| SLC10A2-20-BIO | 20 (40 μL) | 200 μL |  |
Gene Summary
This gene encodes a sodium/bile acid cotransporter. This transporter is the primary mechanism for uptake of intestinal bile acids by apical cells in the distal ileum. Bile acids are the catabolic product of cholesterol metabolism, so this protein is also critical for cholesterol homeostasis. Mutations in this gene cause primary bile acid malabsorption (PBAM); muatations in this gene may also be associated with other diseases of the liver and intestines, such as familial hypertriglyceridemia (FHTG). [provided by RefSeq, Mar 2010]
Gene Details
Gene Symbol: SLC10A2
Gene Name: Solute Carrier Family 10 Member 2
Chromosome: CHR13: 103696347-103719196
Locus: 13q33.1
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: SLC10A2 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: SLC10A2-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping