CCHLND FISH Probe
The CCHLND FISH probe is designed to hybridize to the CCHLND 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 |
|---|---|---|---|---|
| SLC33A1-20-OR (Standard Design) | 20 (40 μL) | 200 μL |  |
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| SLC33A1-20-RE | 20 (40 μL) | 200 μL |  |
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| SLC33A1-20-GO | 20 (40 μL) | 200 μL |  |
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| SLC33A1-20-GR | 20 (40 μL) | 200 μL |  |
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| SLC33A1-20-AQ | 20 (40 μL) | 200 μL |  |
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| SLC33A1-20-DIG | 20 (40 μL) | 200 μL |  |
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| SLC33A1-20-BIO | 20 (40 μL) | 200 μL |  |
Gene Summary
The protein encoded by this gene is required for the formation of O-acetylated (Ac) gangliosides. The encoded protein is predicted to contain 6 to 10 transmembrane domains, and a leucine zipper motif in transmembrane domain III. Defects in this gene have been reported to cause spastic paraplegia autosomal dominant type 42 (SPG42) in one Chinese family, but not in similar patients of European descent. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2010]
Gene Details
Gene Symbol: SLC33A1
Gene Name: Solute Carrier Family 33 Member 1
Chromosome: CHR3: 155544300-155572248
Locus: 3q25.31
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|
Customer Publications
Product Details
Product: CCHLND FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: SLC33A1-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping