AGPS (Human) Recombinant Protein (Q01)
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More Files
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Specification
Product Description
Human AGPS partial ORF ( NP_003650, 559 a.a. - 658 a.a.) recombinant protein with GST-tag at N-terminal.
Sequence
FAPFSTCRVTQTYDAGACIYFYFAFNYRGISDPLTVFEQTEAAAREEILANGGSLSHHHGVGKLRKQWLKESISDVGFGMLKSVKEYVDPNNIFGNRNLL
Host
Wheat Germ (in vitro)
Theoretical MW (kDa)
36.74
Interspecies Antigen Sequence
Mouse (96); Rat (96)
Preparation Method
Purification
Glutathione Sepharose 4 Fast Flow
Quality Control Testing
12.5% SDS-PAGE Stained with Coomassie Blue.
Storage Buffer
50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer.
Storage Instruction
Store at -80°C. Aliquot to avoid repeated freezing and thawing.
Note
Best use within three months from the date of receipt of this protein.
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Applications
Enzyme-linked Immunoabsorbent Assay
Western Blot (Recombinant protein)
Antibody Production
Protein Array
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Gene Info — AGPS
Entrez GeneID
8540GeneBank Accession#
NM_003659Protein Accession#
NP_003650Gene Name
AGPS
Gene Alias
ADAP-S, ADAS, ADHAPS, ADPS, ALDHPSY, DKFZp762O2215, FLJ99755
Gene Description
alkylglycerone phosphate synthase
Gene Ontology
HyperlinkGene Summary
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
Other Designations
aging-associated protein 5|alkyl-DHAP synthase|alkyldihydroxyacetone phosphate synthase|alkyldihydroxyacetonephosphate synthase, peroxisomal
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Interactome
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Pathway
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Disease
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