FVH2 FISH Probe
The FVH2 FISH probe is designed to hybridize to the FVH2 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 |
|---|---|---|---|---|
| SLC38A8-20-OR (Standard Design) | 20 (40 μL) | 200 μL |  |
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| SLC38A8-20-RE | 20 (40 μL) | 200 μL |  |
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| SLC38A8-20-GO | 20 (40 μL) | 200 μL |  |
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| SLC38A8-20-GR | 20 (40 μL) | 200 μL |  |
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| SLC38A8-20-AQ | 20 (40 μL) | 200 μL |  |
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| SLC38A8-20-DIG | 20 (40 μL) | 200 μL |  |
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| SLC38A8-20-BIO | 20 (40 μL) | 200 μL |  |
Gene Summary
This gene encodes a putative sodium-dependent amino-acid/proton antiporter. The protein has eleven transmembrane domains, an extracellular N-terminus and an intracellular C-terminal tail. The protein is a member of the SLC38 sodium-coupled neutral amino acid transporter family of proteins. Mutations in this gene result in foveal hypoplasia with or without optic nerve misrouting and/or anterior segment dysgenesis. [provided by RefSeq, May 2014]
Gene Details
Gene Symbol: SLC38A8
Gene Name: Solute Carrier Family 38 Member 8
Chromosome: CHR16: 84043388-84075762
Locus: 16q23.3
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: FVH2 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: SLC38A8-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping