HJCD FISH Probe
The HJCD FISH probe is designed to hybridize to the HJCD 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 |
---|---|---|---|---|
SLC29A3-20-OR (Standard Design) | 20 (40 μL) | 200 μL | ||
SLC29A3-20-RE | 20 (40 μL) | 200 μL | ||
SLC29A3-20-GO | 20 (40 μL) | 200 μL | ||
SLC29A3-20-GR | 20 (40 μL) | 200 μL | ||
SLC29A3-20-AQ | 20 (40 μL) | 200 μL | ||
SLC29A3-20-DIG | 20 (40 μL) | 200 μL | ||
SLC29A3-20-BIO | 20 (40 μL) | 200 μL |
Gene Summary
This gene encodes a nucleoside transporter. The encoded protein plays a role in cellular uptake of nucleosides, nucleobases, and their related analogs. Mutations in this gene have been associated with H syndrome, which is characterized by cutaneous hyperpigmentation and hypertrichosis, hepatosplenomegaly, heart anomalies, and hypogonadism. A related disorder, PHID (pigmented hypertrichosis with insulin-dependent diabetes mellitus), has also been associated with mutations at this locus. Alternatively spliced transcript variants have been described.[provided by RefSeq, Mar 2010]
Gene Details
Gene Symbol: SLC29A3
Gene Name: Solute Carrier Family 29 Member 3
Chromosome: CHR10: 73079009-73123147
Locus: 10q22.1
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: HJCD FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: SLC29A3-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping