GLDC 抗体
Quick Overview for GLDC 抗体 (ABIN2856747)
抗原
See all GLDC 抗体适用
宿主
克隆类型
标记
应用范围
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交叉反应
- 人, 小鼠, 大鼠
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产品特性
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Rabbit Polyclonal antibody to Glycine dehydrogenase (glycine dehydrogenase (decarboxylating))
Glycine dehydrogenase antibody [N3C2-2], Internal -
纯化方法
- Purified by antigen-affinity chromatography.
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免疫原
- Recombinant protein encompassing a sequence within the center region of human Glycine dehydrogenase. The exact sequence is proprietary.
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亚型
- IgG
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anti-Glycine Dehydrogenase (GLDC) (AA 81-268) antibody
GLDC 适用: 人 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Glycine Dehydrogenase (GLDC) (AA 36-290) antibodyGLDC 适用: 人 WB, IHC, IP, IF 宿主: 兔 Polyclonal unconjugated
anti-Glycine Dehydrogenase (GLDC) (AA 627-833) antibodyGLDC 适用: 人 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Glycine Dehydrogenase (GLDC) (AA 868-984) antibodyGLDC 适用: 人 IHC, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Glycine Dehydrogenase (GLDC) antibodyGLDC 适用: 人, 小鼠, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
anti-Glycine Dehydrogenase (GLDC) (AA 49-77), (N-Term) antibodyGLDC 适用: 人, 小鼠 WB 宿主: 兔 Polyclonal RB23981 unconjugated
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应用备注
- WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. IHC-P: 1:100-1:1000. IP: 1:100-1:500. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
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说明
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Positive Control: HepG2
Validation: Comparison
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 0.46 mg/mL
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缓冲液
- 1XPBS ( pH 7), 1 % BSA, 20 % Glycerol, 0.025 % ProClin 300
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储存液
- ProClin
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注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- 4 °C,-20 °C
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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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- GLDC (Glycine Dehydrogenase (GLDC))
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别名
- glycine decarboxylase
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背景
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The enzyme system for cleavage of glycine (glycine cleavage system, GCS, EC 2.1.2.10), which is confined to the mitochondria, is composed of 4 protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase), H protein (a lipoic acid-containing protein), T protein (a tetrahydrofolate-requiring enzyme), and L protein (a lipoamide dehydrogenase). Glycine encephalopathy (GCE, MIM 605899) may be due to a defect in any one of these enzymes, see MIM 238310, MIM 238330, and MIM 238331.[supplied by OMIM]
Cellular Localization: Mitochondrion -
分子量
- 113 kDa
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基因ID
- 2731
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UniProt
- P23378
抗原
-
