PGD 抗体
Quick Overview for PGD 抗体 (ABIN7384481)
抗原
See all PGD 抗体适用
宿主
克隆类型
标记
应用范围
克隆位点
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纯化方法
- Affinity Purified
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亚型
- IgG
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anti-Phosphogluconate Dehydrogenase (PGD) antibody
PGD 适用: 人 WB, IF, ICC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Phosphogluconate Dehydrogenase (PGD) (AA 184-483) antibodyPGD 适用: 人 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Phosphogluconate Dehydrogenase (PGD) antibodyPGD 适用: 人 WB, IF, IP 宿主: 兔 Monoclonal unconjugated
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 宿主: 兔 Polyclonal 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 4-483) antibodyPGD 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Phosphogluconate Dehydrogenase (PGD) antibodyPGD 适用: 人 WB, IHC, IF, 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
anti-Phosphogluconate Dehydrogenase (PGD) (AA 1-483) antibodyPGD 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
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应用备注
- WB 1:1000-1:2000 IF 1:50-1:200
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限制
- 仅限研究用
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浓度
- 300 μg/mL
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缓冲液
- 50 mM Tris-Glycine( pH 7.4), 0.15M NaCl, 40 % Glycerol, 0.01 % Sodium azide and 0.05 % BSA
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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
- 0610042A05Rik,6 phosphogluconate dehydrogenase,decarboxylating,6-phosphogluconate dehydrogenase,6PGD,6PGD,AU019875,C78335,decarboxylating,OTTMUSP00000011754,Pgd,Phosphogluconate dehydrogenase,RP23-249G3.4,6-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.
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分子量
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Observed_MW: 49kDa
Calculated_MW: 53kDa
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基因ID
- 5226
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UniProt
- P52209
抗原
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