AGPS 抗体 (AA 31-130) (AbBy Fluor® 750)
-
- 抗原 See all AGPS 抗体
- AGPS (Alkylglycerone Phosphate Synthase (AGPS))
-
抗原表位
- AA 31-130
-
适用
- 大鼠
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This AGPS antibody is conjugated to AbBy Fluor® 750
-
应用范围
- Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 大鼠
- 预测反应
- Human,Mouse,Cow,Pig,Horse
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human AGPS/Alkyl-DHAP synthase
- 亚型
- IgG
- Top Product
- Discover our top product AGPS Primary Antibody
-
-
- 应用备注
-
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - 限制
- 仅限研究用
-
- 状态
- Liquid
- 浓度
- 1 μg/μL
- 缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- 有效期
- 12 months
-
- 抗原
- AGPS (Alkylglycerone Phosphate Synthase (AGPS))
- 别名
- AGPS/Alkyl-DHAP synthase (AGPS 产品)
- 别名
- fd16e06 antibody, zgc:56718 antibody, wu:fd16e06 antibody, ADAP-S antibody, ADAS antibody, ADHAPS antibody, ADPS antibody, ALDHPSY antibody, 5832437L22 antibody, 9930035G10Rik antibody, AW123847 antibody, Adaps antibody, Adas antibody, Adhaps antibody, Adps antibody, Aldhpsy antibody, bs2 antibody, Adap-s antibody, Ads antibody, alkylglycerone phosphate synthase antibody, alkylglycerone phosphate synthase L homeolog antibody, agps antibody, AGPS antibody, agps.L antibody, Agps antibody
- 背景
-
Synonyms: AAG5, ADAP-S, ADAS, ADAS_HUMAN, ADHAPS, ADPS, Aging associated gene 5 protein, Aging-associated gene 5 protein, AGPS, ALDHPSY, Alkyl-DHAP synthase, Alkyldihydroxyacetonephosphate synthase, Alkyldihydroxyacetonephosphate synthase, peroxisomal, Alkylglycerone phosphate synthase, Alkylglycerone-phosphate synthase, peroxisomal.
Background: AGPS is a 658 amino acid enzyme that is required for glycerolipid metabolism and ether lipid biosynthesis. Localized to the inner aspect of the peroxisomal membrane, AGPS is likely part of a heterotrimeric complex that is also composed of GNPAT and a modified form of GNPAT. Containing one FAD-binding PCMH-type domain, AGPS utilizes FAD as a cofactor in the synthesis of alkyl-glycerone 3-phophate and a long-chain acid anion from 1-acteyl-glyerone 3-phosphate and a long-chain alcohol. Defects in the gene encoding AGPS results in rhizomelic chondrodysplasia punctata type 3, a disease characterized by vertebral disorders, severe mental retardation, cutaneous lesions, cataracts and rhizomelic shortening of the humerus and femur.
- 基因ID
- 8540
- 途径
- SARS-CoV-2 Protein Interactome
-