RDH5 polyclonal, anti-human, mouse, rat
€388.00
In stock
SKU
BS71604
Background:
This gene encodes an enzyme belonging to the short-chain dehydrogenases/reductases (SDR) family. This retinol dehydrogenase functions to catalyze the final step in the biosynthesis of 11-cis retinaldehyde, which is the universal chromophore of visual pigments. Mutations in this gene cause autosomal recessive fundus albipunctatus, a rare form of night blindness that is characterized by a delay in the regeneration of cone and rod photopigments. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the neighboring upstream BLOC1S1 (biogenesis of lysosomal organelles complex-1, subunit 1) gene.
Alternative Name:
RDH1, 9cRDH, SDR9C5, HSD17B9,
Application Dilution: WB: 1:500 - 1:200, IHC: 1:50 - 1:200
Specificity: RDH5 polyclonal antibody detects endogenous levels of RDH5 protein.
Immunogen:
Recombinant protein of human RDH5
MW: Predicted band size: 35 kDa, Observed band size: Refer to Figures
Swis Prot.: Q92781
Purification & Purity:
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Format:
1mg/ml in PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Storage:
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
For research use only, not for use in diagnostic procedure.
This gene encodes an enzyme belonging to the short-chain dehydrogenases/reductases (SDR) family. This retinol dehydrogenase functions to catalyze the final step in the biosynthesis of 11-cis retinaldehyde, which is the universal chromophore of visual pigments. Mutations in this gene cause autosomal recessive fundus albipunctatus, a rare form of night blindness that is characterized by a delay in the regeneration of cone and rod photopigments. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the neighboring upstream BLOC1S1 (biogenesis of lysosomal organelles complex-1, subunit 1) gene.
Alternative Name:
RDH1, 9cRDH, SDR9C5, HSD17B9,
Application Dilution: WB: 1:500 - 1:200, IHC: 1:50 - 1:200
Specificity: RDH5 polyclonal antibody detects endogenous levels of RDH5 protein.
Immunogen:
Recombinant protein of human RDH5
MW: Predicted band size: 35 kDa, Observed band size: Refer to Figures
Swis Prot.: Q92781
Purification & Purity:
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Format:
1mg/ml in PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Storage:
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
For research use only, not for use in diagnostic procedure.
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