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Rabbit Anti-AGPAT2 Antibody (CSB-PA001450ESR2HU)
Supplier: CUSABIO BIOTECH CO.
1-acyl-sn-glycerol-3-phosphate acyltransferase beta Antibody,1-acylglycerol-3-phosphate O-acyltransferase 2 Antibody,1-AGP acyltransferase 2 Antibody,1-AGPAT 2 Antibody,Lysophosphatidic acid acyltransferase beta Antibody,LPAAT-beta Antibody,AGPAT2 AntibodyMore alternative names for the antibody
1 acyl sn glycerol 3 phosphate acyltransferase beta antibody|1 acylglycerol 3 phosphate O acyltransferase 2 antibody|1 AGP acyltransferase 2 antibody|1 AGPAT2 antibody|1-acyl-sn-glycerol-3-phosphate acyltransferase beta antibody|1-acylglycerol-3-phosphate O-acyltransferase 2 antibody|1-AGP acyltransferase 2 antibody|1-AGPAT 2 antibody|Agpat2 antibody|Berardinelli Seip congenital lipodystrophy antibody|BSCL antibody|BSCL1 antibody|EC 22.214.171.124 antibody|LPAAB antibody|LPAAT beta antibody|LPAAT-beta antibody|Lysophosphatidic acid acyltransferase beta antibody|PLCB_HUMAN antibody
Anti-Agpat2 antibody (ab62599)
Anti-Agpat2 antibody (ab62599)
Recommended applications: ELISA, WB, IHC
Recommended dilution: User optimized
Recommended protocols: check protocols
|Catalogue No.|| |
Recombinant human 1-acyl-sn-glycerol-3-phosphate acyltransferase beta protein (199-278AA)
ELISA, WB, IHC
|Recommended dilution|| |
|Molecular weight|| |
Antigen Affinity Purified
Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.
|Database links|| |
<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=gene&cmd=Retrieve&dopt=Graphics&list_uids=10555" target="_blank">Entrez Gene:10555( Human)</a>, <a href="http://www.ncbi.nlm.nih.gov/omim/603100" target="_blank">Omim:603100( Human)</a>, <a href="http://www.uniprot.org/uniprot/O15120" target="_blank">SwissProt:O15120( Human)</a>, <a href="http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG=Hs&CID=320151" target="_blank">Unigene:320151( Human)</a>
|Protein function|| |
Converts lysophosphatidic acid (LPA) into phosphatidic acid by incorporating an acyl moiety at the sn-2 position of the glycerol backbone. .
|Protein tissue specificity|| |
Expressed predominantly in adipose tissue, pancreas and liver. .
|Involvement in disease|| |
Congenital generalized lipodystrophy 1 (CGL1) [MIM:608594]: An autosomal recessive disorder characterized by a near complete absence of adipose tissue, extreme insulin resistance, hypertriglyceridemia, hepatic steatosis and early onset of diabetes. . Note=The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the 1-acyl-sn-glycerol-3-phosphate acyltransferase family. The HXXXXD motif is essential for acyltransferase activity and may constitute the binding site for the phosphate moiety of the glycerol-3-phosphate.
|Protein cellular localization|| |
Endoplasmic reticulum membrane ; Multi-pass membrane protein .
|Research area|| |
<a href="https://antibodyplus.com/research-areas/">All research areas</a>><a href="https://antibodyplus.com/Synthesis-and-Degradation/">Synthesis and Degradation</a>><a href="https://antibodyplus.com/product-tag/LPAAT/">LPAAT</a><br><a href="https://antibodyplus.com/product-tag/Synthesis-and-Degradation/"> (View all antibody categories related to Synthesis and Degradation)</a>
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CUSABIO BIOTECH CO.
|Product type|| |
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