E-AB-12702
AGPAT2 Polyclonal Antibody
Size
£106.20
Was £118.00
- SKU:
- E-AB-12702
- Additional Names:
- 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-acyl-sn-glycerol-3-phosphate acyltransferase beta,1-acylglycerol-3-phosphate O-acyltransferase 2
- Application:
- WB
- Concentration:
- 0.2 mg/ml
- Purification:
- Affinity Purified
- Storage Conditions:
- -20[o]C Avoid freeze/thaw cycles.
- Supplier:
- Elabscience
- Host:
- Rabbit
- Reactivities:
- Human
- Buffer:
- Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol.
- Immunogen:
- Synthetic peptide of human AGPAT2
- Uniprot:
- O15120
- Synonyms:
- 1-acyl-sn-glycerol-3-phosphate acyltransferase beta;1-acylglycerol-3-phosphate O-acyltransferase 2;1-acylglycerol-3-phosphate O-acyltransferase 2 (lysophosphatidic acid acyltransferase, beta);1-AGP acyltransferase 2;1-AGPAT 2;1-AGPAT2;BSCL;BSCL1;LPAAB;LPAAT-beta;Lysophosphatidic acid acyltransferase beta;lysophosphatidic acid acyltransferase-beta;testicular tissue protein Li 143
- Extra Details:
- 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.
- Shipping Conditions:
- Blue Ice