GRHPR 抗体 (AA 51-150) (Biotin)
Quick Overview for GRHPR 抗体 (AA 51-150) (Biotin) (ABIN6943573)
抗原
See all GRHPR 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 51-150
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交叉反应
- 小鼠
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预测反应
- Human,Rat,Dog,Cow,Sheep,Horse,Chicken,Rabbit
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纯化方法
- Purified by Protein A.
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免疫原
- KLH conjugated synthetic peptide derived from human GRHPR
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亚型
- IgG
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anti-Glyoxylate Reductase/hydroxypyruvate Reductase (GRHPR) (AA 1-328) antibody
GRHPR 适用: 人 WB, ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Glyoxylate Reductase/hydroxypyruvate Reductase (GRHPR) (AA 1-328) antibodyGRHPR 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 4E6-1F2 unconjugated
anti-Glyoxylate Reductase/hydroxypyruvate Reductase (GRHPR) (AA 100-328) antibodyGRHPR 适用: 人 WB, IF 宿主: 兔 Polyclonal unconjugated
anti-Glyoxylate Reductase/hydroxypyruvate Reductase (GRHPR) (N-Term) antibodyGRHPR 适用: 人, 大鼠, 犬, Pig, 马, 兔 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Glyoxylate Reductase/hydroxypyruvate Reductase (GRHPR) (AA 21-54), (N-Term) antibodyGRHPR 适用: 人 WB 宿主: 兔 Polyclonal RB48761 unconjugated
anti-Glyoxylate Reductase/hydroxypyruvate Reductase (GRHPR) (AA 38-87) antibodyGRHPR 适用: 人, 犬, Pig WB 宿主: 兔 Polyclonal unconjugated
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应用备注
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WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500 -
限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 μg/μL
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缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
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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
- -20 °C
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储存方法
- Store at -20°C for 12 months.
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有效期
- 12 months
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- GRHPR (Glyoxylate Reductase/hydroxypyruvate Reductase (GRHPR))
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别名
- GRHPR
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背景
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Synonyms: GLXR, glycerate 2 dehydrogenase, GLYD, Glyoxylate reductase/hydroxypyruvate reductase, Grhpr, GRHPR_HUMAN, OTTHUMP00000021379, OTTHUMP00000021380, OTTHUMP00000046131, PH 2, PH2, Primary hyperoxaluria type 2.
Background: This gene encodes an enzyme with hydroxypyruvate reductase, glyoxylate reductase, and D-glycerate dehydrogenase enzymatic activities. The enzyme has widespread tissue expression and has a role in metabolism. Type II hyperoxaluria is caused by mutations in this gene. [provided by RefSeq, Jul 2008]
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基因ID
- 9380
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UniProt
- Q9UBQ7
抗原
-
