SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
ACOT7-PLEKHG5-20-RERE | 20 (40 μL) | 200 μL | Request Pricing | |
ACOT7-PLEKHG5-20-REOR | 20 (40 μL) | 200 μL | Request Pricing | |
ACOT7-PLEKHG5-20-REGO | 20 (40 μL) | 200 μL | Request Pricing | |
ACOT7-PLEKHG5-20-REGR | 20 (40 μL) | 200 μL | Request Pricing | |
ACOT7-PLEKHG5-20-REAQ | 20 (40 μL) | 200 μL | Request Pricing | |
ACOT7-PLEKHG5-20-ORRE | 20 (40 μL) | 200 μL | Request Pricing | |
ACOT7-PLEKHG5-20-OROR | 20 (40 μL) | 200 μL | Request Pricing | |
ACOT7-PLEKHG5-20-ORGO | 20 (40 μL) | 200 μL | Request Pricing | |
ACOT7-PLEKHG5-20-ORGR | 20 (40 μL) | 200 μL | Request Pricing | |
ACOT7-PLEKHG5-20-ORAQ | 20 (40 μL) | 200 μL | Request Pricing | |
ACOT7-PLEKHG5-20-GORE | 20 (40 μL) | 200 μL | Request Pricing | |
ACOT7-PLEKHG5-20-GOOR | 20 (40 μL) | 200 μL | Request Pricing | |
ACOT7-PLEKHG5-20-GOGO | 20 (40 μL) | 200 μL | Request Pricing | |
ACOT7-PLEKHG5-20-GOGR | 20 (40 μL) | 200 μL | Request Pricing | |
ACOT7-PLEKHG5-20-GOAQ | 20 (40 μL) | 200 μL | Request Pricing | |
ACOT7-PLEKHG5-20-GRRE | 20 (40 μL) | 200 μL | Request Pricing | |
ACOT7-PLEKHG5-20-GROR | 20 (40 μL) | 200 μL | Request Pricing | |
ACOT7-PLEKHG5-20-GRGO | 20 (40 μL) | 200 μL | Request Pricing | |
ACOT7-PLEKHG5-20-GRGR | 20 (40 μL) | 200 μL | Request Pricing | |
ACOT7-PLEKHG5-20-GRAQ | 20 (40 μL) | 200 μL | Request Pricing | |
ACOT7-PLEKHG5-20-AQRE | 20 (40 μL) | 200 μL | Request Pricing | |
ACOT7-PLEKHG5-20-AQOR | 20 (40 μL) | 200 μL | Request Pricing | |
ACOT7-PLEKHG5-20-AQGO | 20 (40 μL) | 200 μL | Request Pricing | |
ACOT7-PLEKHG5-20-AQGR | 20 (40 μL) | 200 μL | Request Pricing | |
ACOT7-PLEKHG5-20-AQAQ | 20 (40 μL) | 200 μL | Request Pricing |
This gene encodes a member of the acyl coenzyme family. The encoded protein hydrolyzes the CoA thioester of palmitoyl-CoA and other long-chain fatty acids. Decreased expression of this gene may be associated with mesial temporal lobe epilepsy. Alternatively spliced transcript variants encoding distinct isoforms with different subcellular locations have been characterized. [provided by RefSeq, Jul 2008]
Gene Symbol : ACOT7
Gene Name : Acyl-CoA thioesterase 7
Chromosome : CHR 1: 639,376,5-626,427,1
Locus : 1p36.31
This gene encodes a protein that activates the nuclear factor kappa B (NFKB1) signaling pathway. Mutations in this gene are associated with autosomal recessive distal spinal muscular atrophy. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2012]
Gene Symbol : PLEKHG5
Gene Name : Pleckstrin homology and RhoGEF domain containing G5
Chromosome : CHR 1: 652,006,0-646,609,1
Locus : 1p36.31
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