PGD 抗体
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北京 101111
Quick Overview for PGD 抗体 (ABIN7269315)
抗原
See all PGD 抗体适用
宿主
克隆类型
标记
应用范围
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原理
- PGD Rabbit mAb
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交叉反应
- 人, 小鼠, 大鼠
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产品特性
- Monoclonal Antibodies
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纯化方法
- Affinity purification
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免疫原
- A synthesized peptide derived from human PGD.
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亚型
- IgG
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anti-Phosphogluconate Dehydrogenase (PGD) (AA 184-483) antibody
PGD 适用: 人 WB, IF, IHC 宿主: 兔 Polyclonal unconjugated
anti-Phosphogluconate Dehydrogenase (PGD) antibodyPGD 适用: 人 WB, IF, ICC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Phosphogluconate Dehydrogenase (PGD) antibodyKD Validated PGD 适用: 人 WB, FACS, IF (p) 宿主: 兔 Monoclonal 25GB3170 unconjugated Recombinant Antibody
anti-Phosphogluconate Dehydrogenase (PGD) (AA 236-265) antibodyPGD 适用: 人, 小鼠 WB, FACS, IHC (p) 宿主: 兔 Polyclonal RB22902 unconjugated
anti-Phosphogluconate Dehydrogenase (PGD) (AA 1-483) antibodyPGD 适用: 人 WB, ELISA, IF, ICC 宿主: 小鼠 Monoclonal AT46B3 unconjugated
anti-Phosphogluconate Dehydrogenase (PGD) (C-Term) antibodyPGD 适用: 人, 小鼠, 大鼠 WB, ELISA, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Phosphogluconate Dehydrogenase (PGD) (AA 1-483) antibodyPGD 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Phosphogluconate Dehydrogenase (PGD) (AA 4-483) antibodyPGD 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Phosphogluconate Dehydrogenase (PGD) antibodyPGD 适用: 人 WB, IF, IHC, IHC (p) 宿主: 小鼠 Monoclonal 2A5 unconjugated
anti-Phosphogluconate Dehydrogenase (PGD) (Internal Region) antibodyPGD 适用: 人, 小鼠, 大鼠 WB, ELISA 宿主: 兔 Polyclonal unconjugated
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应用备注
- WB,1:500 - 1:2000,IF,1:50 - 1:200,IP,1:50 - 1:200
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限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- PGD (Phosphogluconate Dehydrogenase (PGD))
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别名
- PGD
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背景
- 6-phosphogluconate dehydrogenase is the second dehydrogenase in the pentose phosphate shunt. Deficiency of this enzyme is generally asymptomatic, and the inheritance of this disorder is autosomal dominant. Hemolysis results from combined deficiency of 6-phosphogluconate dehydrogenase and 6-phosphogluconolactonase suggesting a synergism of the two enzymopathies. Several transcript variants encoding different isoforms have been found for this gene.,PGD, 6PGD, phosphogluconate dehydrogenase,Signal Transduction,Endocrine & Metabolism,PGD
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分子量
- 45kDa
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基因ID
- 5226
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UniProt
- P52209
抗原
-
