GTX100301
ERAB antibody
Cannot supply to this region.
- SKU:
- GTX100301
- Additional Names:
- hydroxysteroid 17-beta dehydrogenase 10 , 17b-HSD10 , ABAD , CAMR , DUPXp11.22 , ERAB , HADH2 , HCD2 , HSD10MD , MHBD , MRPP2 , MRX17 , MRX31 , MRXS10 , SCHAD , SDR5C1
- Application:
- IHC, WB, IHC-P, IF, ICC
- Concentration:
- 1 mg/ml
- Physical State:
- Liquid
- Species Reactivity:
- Human
- Purification:
- Affinity Purified
- Storage Conditions:
- -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
- Supplier:
- Genetex
- Host:
- Rabbit
- Reactivities:
- Fish, Human, Mouse, Rat
- Buffer:
- PBS, 20% Glycerol, 0.01% Thimerosal.
- Immunogen:
- Carrier-protein conjugated synthetic peptide encompassing a sequence within the C-terminus region of human ERAB. The exact sequence is proprietary.
- Uniprot:
- Q99714
- Synonyms:
- 17-beta-hydroxysteroid dehydrogenase 10;17b-HSD10;2-methyl-3-hydroxybutyryl-CoA dehydrogenase;3-hydroxy-2-methylbutyryl-CoA dehydrogenase;3-hydroxyacyl-CoA dehydrogenase type II;3-hydroxyacyl-CoA dehydrogenase type-2;AB-binding alcohol dehydrogenase;ABAD;amyloid-beta peptide binding alcohol dehydrogenase;CAMR;DUPXp11.22;endoplasmic reticulum-associated amyloid beta-peptide-binding protein;ERAB;HADH2;HCD2;HSD10MD;MHBD;mitochondrial ribonuclease P protein 2;mitochondrial RNase P subunit 2;MRPP2;MRX17;MRX31;MRXS10;SCHAD;SDR5C1;Short chain dehydrogenase/reductase family 5C member 1;short chain L-3-hydroxyacyl-CoA dehydrogenase type 2;short chain type dehydrogenase/reductase XH98G2;Short-chain type dehydrogenase/reductase XH98G2;Type II HADH
- Extra Details:
- This gene encodes 3-hydroxyacyl-CoA dehydrogenase type II, a member of the short-chain dehydrogenase/reductase superfamily. The gene product is a mitochondrial protein that catalyzes the oxidation of a wide variety of fatty acids, alcohols, and steroids. The protein has been implicated in the development of Alzheimer's disease, and mutations in the gene are the cause of 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency (MHBD). Several alternatively spliced transcript variants have been identified, but the full-length nature of only two transcript variants has been determined. [provided by RefSeq]
- Shipping Conditions:
- Blue Ice