GTX32575
EHHADH antibody
Cannot supply to this region.
- SKU:
- GTX32575
- Additional Names:
- enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase , ECHD , FRTS3 , L-PBE , LBFP , LBP , PBFE
- Application:
- WB
- 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:
- Human, Mouse, Rat
- Buffer:
- PBS, 50% Glycerol, 0.02% Sodium azide.
- Immunogen:
- Recombinant fusion protein containing a sequence corresponding to amino acids 444-723 of human EHHADH (NP_001957.2).
- Uniprot:
- Q08426
- Synonyms:
- 3,2-trans-enoyl-CoA isomerase;ECHD;enoyl-CoA, hydratase/3-hydroxyacyl CoA dehydrogenase;enoyl-Coenzyme A, hydratase/3-hydroxyacyl Coenzyme A dehydrogenase;FRTS3;L-3-hydroxyacyl-CoA dehydrogenase;L-bifunctional protein, peroxisomal;L-PBE;LBFP;LBP;MFE1;multifunctional enzyme 1;PBE;PBFE;peroxisomal bifunctional enzyme;peroxisomal enoyl-CoA hydratase
- Extra Details:
- The protein encoded by this gene is a bifunctional enzyme and is one of the four enzymes of the peroxisomal beta-oxidation pathway. The N-terminal region of the encoded protein contains enoyl-CoA hydratase activity while the C-terminal region contains 3-hydroxyacyl-CoA dehydrogenase activity. Defects in this gene are a cause of peroxisomal disorders such as Zellweger syndrome. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]
- Shipping Conditions:
- Blue Ice