PGD 抗体 (AA 1-171)
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北京 101111
Quick Overview for PGD 抗体 (AA 1-171) (ABIN1885683)
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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抗原表位
- AA 1-171
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纯化方法
- Purified by antigen-affinity chromatography.
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免疫原
- Recombinant protein fragment contain a sequence corresponding to a region within amino acids 1 and 171 of Human PGD
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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) antibodyPGD 适用: 人 WB, IF, IP 宿主: 兔 Monoclonal 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
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应用备注
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Suggested dilutions:
Western blotting: 1.500-1.3000
Immunofluorescence: 1.100-1.200 -
限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- 0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.
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储存液
- Thimerosal (Merthiolate)
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注意事项
- Biohazard Informations: This product contains thimerosal which is hazardous.
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储存条件
- 4 °C/-20 °C
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储存方法
- Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
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- PGD (Phosphogluconate Dehydrogenase (PGD))
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别名
- PGD
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背景
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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.[provided by RefSeq]
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分子量
- 53 kDa
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基因ID
- 5226
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NCBI登录号
- NM_002631, NP_002622
抗原
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