CHD5 Break Apart FISH Probe
Empire Genomics’ CHD5 Break Apart FISH Probe is designed to flank the CHD5 gene and is typically used for detecting CHD5 rearrangements such as translocations. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe comes labeled in green and orange by default, but may be customized to meet your needs.
** 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 |
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| CHD5BA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL |
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| CHD5BA-20-AQOR | 20 (40 μL) | 200 μL |
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| CHD5BA-20-GOGR | 20 (40 μL) | 200 μL |
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| CHD5BA-20-GORE | 20 (40 μL) | 200 μL |
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| CHD5BA-20-GRGO | 20 (40 μL) | 200 μL |
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| CHD5BA-20-GRRE | 20 (40 μL) | 200 μL |
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| CHD5BA-20-ORGR | 20 (40 μL) | 200 μL |
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| CHD5BA-20-REGO | 20 (40 μL) | 200 μL |
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| CHD5BA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
This gene is located in the candidate region for congenital heart disease (CHD) in Down syndrome (DS). It encodes a basic protein that functions as a receptor that promotes insertion of tail-anchored proteins in the endoplasmic reticulum membrane. This gene is located at a maternally-methylated differentially methylated region (DMR); however, its transcription may be biallelic, not imprinted. Alternative splicing results in different transcript variants. A pseudogene has been defined on chromosome 4. [provided by RefSeq, Apr 2017]
Gene Details
Gene Symbol: WRB
Gene Name: Tryptophan Rich Basic Protein
Chromosome: CHR21: 40752212-40769815
Locus: 21q22.2
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: CHD5 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: WRB-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping