GTX88923
HADH antibody, Internal
Cannot supply to this region.
- SKU:
- GTX88923
- Additional Names:
- hydroxyacyl-CoA dehydrogenase , HAD , HADH1 , HADHSC , HCDH , HHF4 , MSCHAD , SCHAD
- Application:
- WB
- Concentration:
- 0.50 mg/ml
- Physical State:
- Liquid
- Species Reactivity:
- Human
- Purification:
- Ammonium Sulfate Precipitated; 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:
- Goat
- Reactivities:
- Human
- Buffer:
- TBS, 0.5% BSA, 0.02% Sodium azide.
- Immunogen:
- Peptide with sequence C-YERGDASKEDID, from the internal region of the protein sequence according to NP_005318.2.
- Uniprot:
- Q16836
- Synonyms:
- HAD;HADH1;HADHSC;HCDH;HHF4;hydroxyacyl-coenzyme A dehydrogenase, mitochondrial;L-3-hydroxyacyl-Coenzyme A dehydrogenase, short chain;medium and short-chain L-3-hydroxyacyl-coenzyme A dehydrogenase;MSCHAD;SCHAD;short-chain 3-hydroxyacyl-CoA dehydrogenase;testis secretory sperm-binding protein Li 203a
- Extra Details:
- This gene is a member of the 3-hydroxyacyl-CoA dehydrogenase gene family. The encoded protein functions in the mitochondrial matrix to catalyze the oxidation of straight-chain 3-hydroxyacyl-CoAs as part of the beta-oxidation pathway. Its enzymatic activity is highest with medium-chain-length fatty acids. Mutations in this gene cause one form of familial hyperinsulinemic hypoglycemia. The human genome contains a related pseudogene of this gene on chromosome 15. [provided by RefSeq, May 2010]
- Shipping Conditions:
- Blue Ice