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查看说明书Alkyl-DHAP synthase Rabbit pAb
Cat#:DPA03619应用：WB,IHC,FC,IP
| Product Name: | Alkyl-DHAP synthase Rabbit pAb |
| Cat No.: | DPA03619 |
| Clonality: | Polyclonal |
| Species Reactivity: | Human, Mouse, Rat |
| Tested Applications: | WB,IHC,FC,IP |
| Recommended Dilution: | WB: 1:1000-1:5000 IHC: 1:20 FC: 1:20 IP: 1:20 |
| Size: | 30ul 50ul 100uL |
| Format: | Liquid |
| Source: | Rabbit |
| Purification Method: | Affinity Purification |
| Isotype: | IgG |
| Conjugate: | Un-conjugated |
| Storage: | Store at -20°C. Supplied in 50nM Tris-Glycine(pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide a |
| Immunogen: | Recombinant protein of human Alkyl-DHAP synthase |
| Calculated Molecular Weight: | 73 kDa |
| Observed Molecular Weight: | 73 kDa |
| GenBank Accession Number: | O00116 |
| Gene ID (NCBI): | 8540 |
| Synonyms: | ADAS; ADPS; RCDP3; ADAP-S; ADHAPS; ALDHPSY |
| Background: | 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] |
| Category: | Primary Ab |
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