GTX101396
Alkyl-DHAP synthase antibody
Cannot supply to this region.
- SKU:
- GTX101396
- Additional Names:
- alkylglycerone phosphate synthase , ADAP-S , ADAS , ADHAPS , ADPS , ALDHPSY , RCDP3
- Application:
- WB
- 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:
- Human
- Buffer:
- PBS, 20% Glycerol, 0.025% ProClin 300.
- Immunogen:
- Recombinant protein encompassing a sequence within the center region of human Alkyl-DHAP synthase. The exact sequence is proprietary.
- Uniprot:
- O00116
- Synonyms:
- ADAP-S;ADAS;ADHAPS;ADPS;aging-associated gene 5 protein;aging-associated protein 5;ALDHPSY;alkyl-DHAP synthase;alkyldihydroxyacetonephosphate synthase, peroxisomal;Alkylglycerone-phosphate synthase;RCDP3
- Extra Details:
- This gene is a member of the FAD-binding oxidoreductase/transferase type 4 family. It encodes a protein that catalyzes the second step of ether lipid biosynthesis in which acyl-dihydroxyacetonephosphate (DHAP) is converted to alkyl-DHAP by the addition of a long chain alcohol and the removal of a long-chain acid anion. The protein is localized to the inner aspect of the peroxisomal membrane and requires FAD as a cofactor. Mutations in this gene have been associated with rhizomelic chondrodysplasia punctata, type 3 and Zellweger syndrome. [provided by RefSeq]
- Shipping Conditions:
- Blue Ice