ELOVL4 rabbit pAb
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ELOVL4 rabbit pAb
Background :
This gene encodes a membrane-bound protein which is a member of the ELO family, proteins which participate in the biosynthesis of fatty acids. Consistent with the expression of the encoded protein in photoreceptor cells of the retina, mutations and small deletions in this gene are associated with Stargardt-like macular dystrophy (STGD3) and autosomal dominant Stargardt-like macular dystrophy (ADMD), also referred to as autosomal dominant atrophic macular degeneration. [provided by RefSeq, Jul 2008]Description :
This gene encodes a membrane-bound protein which is a member of the ELO family, proteins which participate in the biosynthesis of fatty acids. Consistent with the expression of the encoded protein in photoreceptor cells of the retina, mutations and small deletions in this gene are associated with Stargardt-like macular dystrophy (STGD3) and autosomal dominant Stargardt-like macular dystrophy (ADMD), also referred to as autosomal dominant atrophic macular degeneration. [provided by RefSeq, Jul 2008],Product Name Alternative :
ELOVL4; Elongation of very long chain fatty acids protein 4; 3-keto acyl-CoA synthase ELOVL4; ELOVL fatty acid elongase 4; ELOVL FA elongase 4UniProt :
Q9GZR5Swiss Prot :
Q9GZR5Reactivity :
Human; MouseImmunogen :
The antiserum was produced against synthesized peptide derived from human ELOVL4. AA range:41-90Target :
ELOVL4Clonality :
PolyclonalSource :
RabbitApplications :
WB; ELISAConcentration :
1 mg/mlDilution :
Western Blot: 1/500 - 1/2000. ELISA: 1/40000. Not yet tested in other applications.Buffer :
-20°C/1 yearMolecular Weight :
37kDStorage Conditions :
-20°C/1 yearObserved Molecular Weight :
37kDFragment :
IgGSubcellular Location :
Endoplasmic reticulum membrane ; Multi-pass membrane protein .Other Product Names :
ELOVL4; Elongation of very long chain fatty acids protein 4; 3-keto acyl-CoA synthase ELOVL4; ELOVL fatty acid elongase 4; ELOVL FA elongase 4Gene ID (Human) :
6785

