ACSL6 rabbit pAb

The protein encoded by this gene catalyzes the formation of acyl-CoA from fatty acids, ATP, and CoA, using magnesium as a cofactor. The encoded protein plays a major role in fatty acid metabolism in the brain. Translocations with the ETV6 gene are causes of myelodysplastic syndrome with basophilia, acute myelogenous leukemia with eosinophilia, and acute eosinophilic leukemia. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2011],

ACSL6; ACS2; FACL6; KIAA0837; LACS5; Long-chain-fatty-acid--CoA ligase 6; Long-chain acyl-CoA synthetase 6; LACS 6

23305

Q9UKU0

Mitochondrion outer membrane ; Single-pass type III membrane protein. Peroxisome membrane ; Single-pass type III membrane protein. Microsome membrane ; Single-pass type III membrane protein. Endoplasmic reticulum membrane ; Single-pass type III membrane protein.

Rabbit

Human, Mouse, Rat

The antiserum was produced against synthesized peptide derived from human ACSL6. AA range:499-548

Polyclonal

WB, IHC, IF, ELISA

1 year

1 mg/mL

Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. ELISA: 1/40000. Not yet tested in other applications.

78kD

PBS with 0.02% sodium azide and 50% glycerol pH 7.4. Store at -20°C. Avoid repeated freeze-thaw cycles.