AGPAT2 Polyclonal Antibody
| 规格： | / 20μL / 60μL / 120μL / 200μL |
| 价格： | / ￥420 / ￥1010 / ￥1640 / ￥2365 |
货号：E-AB-12702
宿主: Rabbit
反应性: H
应用: WB
Overview
| 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 2.3.1.51,LPAAB,LPAAT beta,LPAAT-beta,Lysophosphatidic acid acyltransferase beta,PLCB,AGPAT2抗体 |
| Swissprot | O15120 |
| Source | Rabbit |
| Reactivity | Human |
| Immunogen | Synthetic peptide of human AGPAT2 |
| Application | WB(Detection kit: E-IR-R304) |
| Recommended dilution | WB,,1:500-1:2000; |
| Concentration | 0.2 mg/mL |
| Clonality | Polyclonal |
Properties
| Cellular localization | Membrane. |
| Tissue specificity | Expressed predominantly in heart and liver. |
| 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. |
