RDH5 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA530150-Each-of-1 | In Stock | ₹ 46,502.50 |
PIPA530150 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 46,502.50
GST (18%): ₹ 8,370.45
Total Price: ₹ 54,872.95
Antigen
RDH5
Classification
Polyclonal
Conjugate
Unconjugated
Gene
RDH5
Gene Alias
11-cis RDH; 11-cis retinol dehydrogenase; 11-cis RoDH; 9-cis; 9-cis retinol dehydrogenase; 9-cis-retinol dehydrogenase; 9-cis-retinol specific dehydrogenase; 9cRDH; AI987873; Cis-retinol dehydrogenase; cRDH; FLJ39337; FLJ97089; HSD17B9; rdh; RDH1; Rdh4; rdh5; retinol dehydrogenase 1; retinol dehydrogenase 5; retinol dehydrogenase 5 (11-cis and 9-cis); retinol dehydrogenase 5 (11-cis/9-cis); retinol dehydrogenase type 5; SDR9C5; Short chain dehydrogenase/reductase family 9C member 5; short chain dehydrogenase/reductase family 9C, member 5
Host Species
Rabbit
Purification Method
Antigen affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
5959
Content And Storage
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Form
Liquid
Applications
Immunohistochemistry (Paraffin), Western Blot
Concentration
1 mg/mL
Formulation
0.1M tris glycine with 20% glycerol and 0.01% thimerosal; pH 7
Gene Accession No.
Q92781
Gene Symbols
RDH5
Immunogen
Recombinant fragment corresponding to a region within amino acids 60 and 276 of Human RDH5
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human
Product Type
Antibody
Isotype
IgG
Related Products
Description
- Recommended positive controls: A549, HeLa, Jurkat, NT2D1
- Predicted reactivity: Mouse (89%), Bovine (92%)
- Store product as a concentrated solution
- Centrifuge briefly prior to opening the vial
- This gene encodes an enzyme belonging to the short-chain dehydrogenases/reductases 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 gene.