Product Description
RDH5 polyclonal antibody is available at gentaur for next week delivery
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.
Applications: WB IHC
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).
Storage&Stability: Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
Specificity: RDH5 polyclonal antibody detects endogenous levels of RDH5 protein.
W4BiowMW: ~ 38 kDa
Reactivity: Human,Mouse,Rat
Note: For research use only, not for use in diagnostic procedure.
Immunogen:
Recombinant protein of human RDH5Alternative Name:
RDH1; 9cRDH; SDR9C5; HSD17B9;Western blot analysis: Western blot analysis of extracts of various cells, using RDH5 antibody.
Immunohistochemistry: Immunofluorescence analysis of rat retina using RDH5 Polyclonal Antibody.
Immunofluorescence analysis:
Host: Rabbit
Swiss-Prot: Q92781
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