Metabolism Antibodies 3
Anti-RDH5 Antibody (CAB8055)
- SKU:
- CAB8055
- Product Type:
- Antibody
- Applications:
- WB
- Applications:
- IHC
- Reactivity:
- Human
- Reactivity:
- Mouse
- Reactivity:
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Research Area:
- Metabolism
Description
Antibody Name: | RDH5 Rabbit Polyclonal Antibody |
Antibody SKU: | CAB8055 |
Antibody Size: | 20uL, 50uL, 100uL |
Application: | WB IHC IF |
Reactivity: | Human, Mouse, Rat |
Host Species: | Rabbit |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 24-318 of human RDH5 (NP_002896.2). |
Application: | WB IHC IF |
Recommended Dilution: | WB 1:500 - 1:2000 IHC 1:50 - 1:100 IF 1:50 - 1:100 |
Reactivity: | Human, Mouse, Rat |
Positive Samples: | A-549, BT-474, Mouse liver, Mouse kidney, Rat liver |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 24-318 of human RDH5 (NP_002896.2). |
Purification Method: | Affinity purification |
Storage Buffer: | Store at -20'C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
Isotype: | IgG |
Sequence: | LPAS NAFV FITG CDSG FGRL LALQ LDQR GFRV LASC LTPS GAED LQRV ASSR LHTT LLDI TDPQ SVQQ AAKW VEMH VKEA GLFG LVNN AGVA GIIG PTPW LTRD DFQR VLNV NTMG PIGV TLAL LPLL QQAR GRVI NITS VLGR LAAN GGGY CVSK FGLE AFSD SLRR DVAH FGIR VSIV EPGF FRTP VTNL ESLE KTLQ ACWA RLPP ATQA HYGG AFLT KYLK MQQR IMNL ICDP DLTK VSRC LEHA LTAR HPRT RYSP GWDA KLLW LPAS YLPA SLVD AVLT WVLP KPAQ AVY |
Gene ID: | 5959 |
Uniprot: | Q92781 |
Cellular Location: | Endoplasmic reticulum lumen, Membrane, Peripheral membrane protein |
Calculated MW: | 34kDa |
Observed MW: | 38kDa |
Synonyms: | RDH5, 9cRDH, HSD17B9, RDH1, SDR9C5 |
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. |
UniProt Protein Function: | RDH5: Stereospecific 11-cis retinol dehydrogenase, which catalyzes the final step in the biosynthesis of 11-cis retinaldehyde, the universal chromophore of visual pigments. Also able to oxidize 9-cis-retinol and 13-cis-retinol, but not all- trans-retinol. Active in the presence of NAD as cofactor but not in the presence of NADP. Defects in RDH5 are a cause of retinitis punctata albescens (RPA); also known as fundus albipunctatus (FA). RPA is a rare form of stationary night blindness characterized by a delay in the regeneration of cone and rod photopigments. Belongs to the short-chain dehydrogenases/reductases (SDR) family. |
UniProt Protein Details: | Protein type:Cofactor and Vitamin Metabolism - retinol; Endoplasmic reticulum; Oxidoreductase; EC 1.1.1.315 Chromosomal Location of Human Ortholog: 12q13-q14 Cellular Component: endoplasmic reticulum membrane; endoplasmic reticulum lumen Molecular Function:retinol dehydrogenase activity Biological Process: phototransduction, visible light; visual perception; retinol metabolic process; retinoid metabolic process Disease: Fundus Albipunctatus |
NCBI Summary: | 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. [provided by RefSeq, Dec 2010] |
UniProt Code: | Q92781 |
NCBI GenInfo Identifier: | 2492753 |
NCBI Gene ID: | 5959 |
NCBI Accession: | Q92781.1 |
UniProt Secondary Accession: | Q92781,O00179, Q8TAI2, |
UniProt Related Accession: | Q92781 |
Molecular Weight: | 34,979 Da |
NCBI Full Name: | 11-cis retinol dehydrogenase |
NCBI Synonym Full Names: | retinol dehydrogenase 5 (11-cis/9-cis) |
NCBI Official Symbol: | RDH5 |
NCBI Official Synonym Symbols: | RDH1; 9cRDH; SDR9C5; HSD17B9 |
NCBI Protein Information: | 11-cis retinol dehydrogenase; 11-cis RDH; 11-cis RoDH; retinol dehydrogenase 1; 9-cis retinol dehydrogenase; 9-cis-retinol specific dehydrogenase; retinol dehydrogenase 5 (11-cis and 9-cis); short chain dehydrogenase/reductase family 9C, member 5 |
UniProt Protein Name: | 11-cis retinol dehydrogenase |
UniProt Synonym Protein Names: | 9-cis retinol dehydrogenase; 9cRDH |
Protein Family: | 11-cis retinol dehydrogenase |
UniProt Gene Name: | RDH5 |
UniProt Entry Name: | RDH1_HUMAN |
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