![Alkyl-DHAP synthase antibody [AGPS-03]](https://www.genetex.com/upload/website/prouct_img/normal/GTX00518/GTX00518_20191028_WB_1_w_23053121_463.webp)
GTX00518
Alkyl-DHAP synthase antibody [AGPS-03]
Cannot supply to this region.
- SKU:
- GTX00518
- Additional Names:
- ADAPS , ADAS , ADHAPS , ADPS , AGPS , ALDHPSY , RCDP3 , alkylglycerone phosphate synthase , Alkyl-DHAP synthase
- Application:
- Flow Cytometry, WB
- Concentration:
- 1 mg/ml
- Physical State:
- Liquid
- Species Reactivity:
- Human
- Purification:
- Protein A Purified
- Storage Conditions:
- 2-8[o]C Do not freeze.
- Supplier:
- Genetex
- Host:
- Mouse
- Reactivities:
- Human
- Buffer:
- PBS, 15mM Sodium azide.
- Immunogen:
- recombinant human AGPS (amino acids 158-384)
- Clone:
- AGPS-03
- 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, Jul 2008]
- Shipping Conditions:
- Blue Ice