SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
ACSF3-ZNF483-20-RERE | 20 (40 μL) | 200 μL | Request Pricing | |
ACSF3-ZNF483-20-REOR | 20 (40 μL) | 200 μL | Request Pricing | |
ACSF3-ZNF483-20-REGO | 20 (40 μL) | 200 μL | Request Pricing | |
ACSF3-ZNF483-20-REGR | 20 (40 μL) | 200 μL | Request Pricing | |
ACSF3-ZNF483-20-REAQ | 20 (40 μL) | 200 μL | Request Pricing | |
ACSF3-ZNF483-20-ORRE | 20 (40 μL) | 200 μL | Request Pricing | |
ACSF3-ZNF483-20-OROR | 20 (40 μL) | 200 μL | Request Pricing | |
ACSF3-ZNF483-20-ORGO | 20 (40 μL) | 200 μL | Request Pricing | |
ACSF3-ZNF483-20-ORGR | 20 (40 μL) | 200 μL | Request Pricing | |
ACSF3-ZNF483-20-ORAQ | 20 (40 μL) | 200 μL | Request Pricing | |
ACSF3-ZNF483-20-GORE | 20 (40 μL) | 200 μL | Request Pricing | |
ACSF3-ZNF483-20-GOOR | 20 (40 μL) | 200 μL | Request Pricing | |
ACSF3-ZNF483-20-GOGO | 20 (40 μL) | 200 μL | Request Pricing | |
ACSF3-ZNF483-20-GOGR | 20 (40 μL) | 200 μL | Request Pricing | |
ACSF3-ZNF483-20-GOAQ | 20 (40 μL) | 200 μL | Request Pricing | |
ACSF3-ZNF483-20-GRRE | 20 (40 μL) | 200 μL | Request Pricing | |
ACSF3-ZNF483-20-GROR | 20 (40 μL) | 200 μL | Request Pricing | |
ACSF3-ZNF483-20-GRGO | 20 (40 μL) | 200 μL | Request Pricing | |
ACSF3-ZNF483-20-GRGR | 20 (40 μL) | 200 μL | Request Pricing | |
ACSF3-ZNF483-20-GRAQ | 20 (40 μL) | 200 μL | Request Pricing | |
ACSF3-ZNF483-20-AQRE | 20 (40 μL) | 200 μL | Request Pricing | |
ACSF3-ZNF483-20-AQOR | 20 (40 μL) | 200 μL | Request Pricing | |
ACSF3-ZNF483-20-AQGO | 20 (40 μL) | 200 μL | Request Pricing | |
ACSF3-ZNF483-20-AQGR | 20 (40 μL) | 200 μL | Request Pricing | |
ACSF3-ZNF483-20-AQAQ | 20 (40 μL) | 200 μL | Request Pricing |
Gene Symbol : ZNF483
Gene Name : Zinc finger protein 483
Chromosome : CHR 9: 111,525,158-111,577,843
Locus : 9q31.3
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 Symbol : ACSF3
Gene Name : Acyl-CoA synthetase family member 3
Chromosome : CHR 16: 890,938,08-891,605,55
Locus : 16q24.3
Lorem Ipsum is simply dummy text of the printing and typesetting industry.
Lorem Ipsum is simply dummy text of the printing and typesetting industry.