AGPAT2 Polyclonal Antibody

Rs. 16,500.00
SKU E-AB-12702


Synonyms 1 acyl sn glycerol 3 phosphate acyltransferase beta,1 acylglycerol 3 phosphate O acyltransferase 2,1 AGP acyltransferase 2,1 AGPAT2,1-acyl-sn-glycerol-3-phosphate acyltransferase beta,1-acylglycerol-3-phosphate O-acyltransferase 2,1-AGP acyltransferase 2,1-AGPAT 2,Agpat2,Berardinelli Seip congenital lipodystrophy,BSCL,BSCL1,EC,LPAAB,LPAAT beta,LPAAT-beta,Lysophosphatidic acid acyltransferase beta,PLCB
Swissprot O15120
Source Rabbit
Reactivity Human
Immunogen Synthetic peptide of human AGPAT2
Application WB,ELISA
Recommended dilution WB 1:500-1:2000
Concentration 0.2mg/mL
Clonality Polyclonal


Cellular localization  
Tissue specificity  
Isotype IgG
Purification Affinity purification
Conjugation Unconjugated
Storage instructions Store at -20℃. Avoid freeze / thaw cycles.
Storage buffer PBS with 0.05% sodium azide, 50% glycerol, PH7.3
Background This gene encodes a member of the 1-acylglycerol-3-phosphate O-acyltransferase family. The protein is located within the endoplasmic reticulum membrane and converts lysophosphatidic acid to phosphatidic acid, the second step in de novo phospholipid biosynthesis. Mutations in this gene have been associated with congenital generalized lipodystrophy (CGL), or Berardinelli-Seip syndrome, a disease characterized by a near absence of adipose tissue and severe insulin resistance. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.


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