HAGHL 抗体 (AA 1-100) (Cy7)
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- 抗原 See all HAGHL 抗体
- HAGHL (Hydroxyacylglutathione Hydrolase-Like (HAGHL))
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抗原表位
- AA 1-100
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适用
- 人, 小鼠
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This HAGHL antibody is conjugated to Cy7
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应用范围
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 人, 小鼠
- 预测反应
- Rat,Dog,Cow,Sheep,Pig,Horse
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human HAGHL
- 亚型
- IgG
- Top Product
- Discover our top product HAGHL Primary Antibody
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anti-Hydroxyacylglutathione Hydrolase-Like (HAGHL) (AA 183-282) antibody
HAGHL 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 5B12 unconjugated
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- 应用备注
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 μg/μL
- 缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- 有效期
- 12 months
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- 抗原
- HAGHL (Hydroxyacylglutathione Hydrolase-Like (HAGHL))
- 别名
- HAGHL (HAGHL 产品)
- 别名
- 1500017E18Rik antibody, 2810014I23Rik antibody, C330022E15Rik antibody, hydroxyacylglutathione hydrolase-like antibody, hydroxyacylglutathione hydrolase like antibody, Haghl antibody, HAGHL antibody
- 背景
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Synonyms: HAGHL, HAGHL_HUMAN, Hydroxyacylglutathione hydrolase-like, Hydroxyacylglutathione hydrolase-like protein.
Background: The hydroxyacylglutathione hydrolase-like protein (HAGHL) is a 290 amino acid protein that belongs to the glyoxalase II family. HAGHL binds two zinc ions per subunit and acts as a hydrolase on ester bonds. The gene encoding HAGHL maps to human chromosome 16, which encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3 % of human cellular DNA and is associated with a variety of genetic disorders. The rare disorder Rubinstein-Taybi syndrome is associated with chromosome 16, as is Crohn's disease, a gastrointestinal inflammatory condition that may involve the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.
- 基因ID
- 84264
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