CYP4V2 rabbit pAb
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CYP4V2 rabbit pAb
Background :
This gene encodes a member of the cytochrome P450 hemethiolate protein superfamily which are involved in oxidizing various substrates in the metabolic pathway. It is implicated in the metabolism of fatty acid precursors into n-3 polyunsaturated fatty acids. Mutations in this gene result in Bietti crystalline corneoretinal dystrophy. [provided by RefSeq, Jul 2008]Description :
This gene encodes a member of the Cytochrome P450 hemethiolate protein superfamily which are involved in oxidizing various substrates in the metabolic pathway. It is implicated in the metabolism of fatty acid precursors into n-3 polyunsaturated fatty acids. Mutations in this gene result in Bietti crystalline corneoretinal dystrophy. [provided by RefSeq, Jul 2008],UniProt :
Q6ZWL3Swiss Prot :
Q6ZWL3Reactivity :
Human; Rat; MouseImmunogen :
Synthesized peptide derived from the Internal region of human CYP4V2.Clonality :
PolyclonalSource :
RabbitApplications :
WB; IHC; IF; ELISAConcentration :
1 mg/mlDilution :
Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. ELISA: 1/20000. Not yet tested in other applications.Molecular Weight :
60kDStorage Conditions :
-20°C/1 yearObserved Molecular Weight :
60kDFragment :
IgGSubcellular Location :
Endoplasmic reticulum membrane ; Single-pass membrane protein .Other Product Names :
CYP4V2; Cytochrome P450 4V2Gene ID (Human) :
285440

