GTX46672
AGPAT2 antibody, C-term
Cannot supply to this region.
- SKU:
- GTX46672
- Additional Names:
- 1-acylglycerol-3-phosphate O-acyltransferase 2 , 1-AGPAT2 , BSCL , BSCL1 , LPAAB , LPAAT-beta
- Application:
- WB
- Concentration:
- 0.5-1 mg/ml
- Physical State:
- Liquid
- Species Reactivity:
- Human
- Purification:
- Protein A Purified
- Storage Conditions:
- -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
- Supplier:
- Genetex
- Host:
- Rabbit
- Reactivities:
- Human
- Buffer:
- PBS, 2% Sucrose, 0.09% Sodium azide.
- Immunogen:
- A synthetic peptide corresponding to a C-terminal region 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. [provided by RefSeq, Jul 2008]
- Shipping Conditions:
- Blue Ice