AGPAT2 antibody
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- Target See all AGPAT2 Antibodies
- AGPAT2 (1-Acylglycerol-3-Phosphate O-Acyltransferase 2 (Lysophosphatidic Acid Acyltransferase, Beta) (AGPAT2))
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Reactivity
- Human, Mouse
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This AGPAT2 antibody is un-conjugated
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Application
- Western Blotting (WB), Immunofluorescence (IF)
- Characteristics
- Polyclonal Antibody
- Purification
- Affinity purification
- Immunogen
- Recombinant fusion protein of human AGPAT2 (NP_006403.2).
- Isotype
- IgG
- Top Product
- Discover our top product AGPAT2 Primary Antibody
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- Application Notes
- WB 1:500-1:2000 IF 1:50-1:100
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 mg/mL
- Buffer
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
- Preservative
- Sodium azide
- Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Storage
- -20 °C
- Storage Comment
- Store at -20°C. Avoid freeze / thaw cycles.
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- Target
- AGPAT2 (1-Acylglycerol-3-Phosphate O-Acyltransferase 2 (Lysophosphatidic Acid Acyltransferase, Beta) (AGPAT2))
- Alternative Name
- AGPAT2 (AGPAT2 Products)
- Synonyms
- AGPAT2 antibody, zgc:153984 antibody, 1-agpat2 antibody, bscl antibody, bscl1 antibody, lpaab antibody, lpaat-beta antibody, 1-AGPAT2 antibody, BSCL antibody, BSCL1 antibody, LPAAB antibody, LPAAT-beta antibody, 2510002J07Rik antibody, AV000834 antibody, 1-acylglycerol-3-phosphate O-acyltransferase 2 antibody, 1-acylglycerol-3-phosphate O-acyltransferase 2 (lysophosphatidic acid acyltransferase, beta) antibody, AGPAT2 antibody, agpat2 antibody, Agpat2 antibody
- 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.
- Molecular Weight
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Observed_MW: 31 kDa
Calculated_MW: 27 kDa/30 kDa
- Gene ID
- 10555
- UniProt
- O15120
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