ACSF3 Break Apart FISH Probe
Empire Genomics’ ACSF3 Break Apart FISH Probe is designed to flank the ACSF3 gene and is typically used for detecting ACSF3 rearrangements such as translocations. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe comes labeled in orange and green 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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ACSF3BA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
ACSF3BA-20-AQOR | 20 (40 μL) | 200 μL | ||
ACSF3BA-20-GOGR | 20 (40 μL) | 200 μL | ||
ACSF3BA-20-GORE | 20 (40 μL) | 200 μL | ||
ACSF3BA-20-GRGO | 20 (40 μL) | 200 μL | ||
ACSF3BA-20-GROR | 20 (40 μL) | 200 μL | ||
ACSF3BA-20-GRRE | 20 (40 μL) | 200 μL | ||
ACSF3BA-20-REGO | 20 (40 μL) | 200 μL | ||
ACSF3BA-20-REGR | 20 (40 μL) | 200 μL |
Gene Summary
This gene encodes a member of the acyl-CoA synthetase family of enzymes that activate fatty acids by catalyzing the formation of a thioester linkage between fatty acids and coenzyme A. The encoded protein is localized to mitochondria, has high specificity for malonate and methylmalonate and possesses malonyl-CoA synthetase activity. Mutations in this gene are a cause of combined malonic and methylmalonic aciduria. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Sep 2013]
Gene Details
Gene Symbol: ACSF3
Gene Name: Acyl-CoA Synthetase Family Member 3
Chromosome: CHR16: 89160216-89222171
Locus: 16q24.3
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: ACSF3 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: ACSF3-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping