ST3GAL5 抗体
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- 抗原 See all ST3GAL5 抗体
- ST3GAL5 (ST3 beta-Galactoside alpha-2,3-Sialyltransferase 5 (ST3GAL5))
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适用
- 人
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This ST3GAL5 antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 交叉反应
- 人
- 产品特性
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Rabbit Polyclonal antibody to ST3GAL5 (ST3 beta-galactoside alpha-2,3-sialyltransferase 5)
ST3GAL5 antibody - 纯化方法
- Purified by antigen-affinity chromatography.
- 免疫原
- Recombinant protein encompassing a sequence within the center region of human ST3GAL5. The exact sequence is proprietary.
- 亚型
- IgG
- Top Product
- Discover our top product ST3GAL5 Primary Antibody
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- 应用备注
- WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
- 说明
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Positive Control: U87-MG
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 mg/mL
- 缓冲液
- 1XPBS ( pH 7), 20 % Glycerol, 0.01 % Thimerosal
- 储存液
- Thimerosal (Merthiolate)
- 注意事项
- This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- 4 °C,-20 °C
- 储存方法
- Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
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- 抗原
- ST3GAL5 (ST3 beta-Galactoside alpha-2,3-Sialyltransferase 5 (ST3GAL5))
- 别名
- ST3 beta-galactoside alpha-2,3-sialyltransferase 5 (ST3GAL5 产品)
- 别名
- SATI antibody, SIAT9 antibody, SIATGM3S antibody, ST3GalV antibody, ST3GAL-V antibody, 3S-T antibody, Siat9 antibody, [a]2 antibody, ST3 beta-galactoside alpha-2,3-sialyltransferase 5 antibody, ST3GAL5 antibody, St3gal5 antibody
- 背景
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Ganglioside GM3 is known to participate in the induction of cell differentiation, modulation of cell proliferation, maintenance of fibroblast morphology, signal transduction, and integrin-mediated cell adhesion. The protein encoded by this gene is a type II membrane protein which catalyzes the formation of GM3 using lactosylceramide as the substrate. The encoded protein is a member of glycosyltransferase family 29 and may be localized to the Golgi apparatus. Mutation in this gene has been associated with Amish infantile epilepsy syndrome. Transcript variants encoding different isoforms have been found for this gene.
Cellular Localization: Golgi apparatus membrane, Single-pass type II membrane protein - 分子量
- 48 kDa
- 基因ID
- 8869
- UniProt
- Q9UNP4
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