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    HAGHL Rabbit pAb (bs-8414R)  
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    產(chǎn)品編號 bs-8414R
    英文名稱(chēng) HAGHL Rabbit pAb
    中文名稱(chēng) 羥基酰谷胱甘肽水解酶樣蛋白抗體
    別    名 HAGHL; HAGHL_HUMAN; Hydroxyacylglutathione hydrolase-like; Hydroxyacylglutathione hydrolase-like protein.  
    研究領(lǐng)域 腫瘤  細胞生物  免疫學(xué)  神經(jīng)生物學(xué)  信號轉導  Alzheimer's  
    抗體來(lái)源 Rabbit
    克隆類(lèi)型 Polyclonal
    克 隆 號
    交叉反應 Human,Mouse (predicted: Rat,Pig,Sheep,Cow,Dog,Horse)
    產(chǎn)品應用 WB=1:500-2000
    not yet tested in other applications.
    optimal dilutions/concentrations should be determined by the end user.
    理論分子量 32 kDa
    檢測分子量
    細胞定位 細胞漿 
    性    狀 Liquid
    濃    度 1mg/ml
    免 疫 原 KLH conjugated synthetic peptide derived from human HAGHL: 1-100/290 
    亞    型 IgG
    純化方法 affinity purified by Protein A
    緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
    保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
    注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
    PubMed PubMed
    產(chǎn)品介紹 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.

    Function:
    Hydroxyacylglutathione hydrolase (HAGH) is a thiolesterase which hydrolyses S-lactoyl-glutathione to reduced glutathione and D-lactate.

    Subcellular Location:
    Cytoplasmic and Mitochondrial

    Similarity:
    Belongs to the metallo-beta-lactamase superfamily. Glyoxalase II family.

    SWISS:
    Q6PII5

    Gene ID:
    84264

    Database links:

    Entrez Gene: 84264 Human

    SwissProt: Q6PII5 Human

    Unigene: 124015 Human



    克羅恩病(節段性腸炎)Crohn’s disease(segmental enteritis”,曾稱(chēng):克隆病)的研究。
    產(chǎn)品圖片
    Sample: Testis(Mouse) Lysate at 40 ug Primary: Anti- HAGHL (bs-8414R) at 1/300 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 32 kD Observed band size: 32 kD
    Sample: MCF-7(Human) Cell Lysate at 40 ug Primary: Anti- HAGHL (bs-8414R) at 1/300 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 32 kD Observed band size: 32 kD
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