TMEM87B Antibody
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中文名稱:TMEM87B兔多克隆抗體
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貨號:CSB-PA023891LA01HU
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規(guī)格:¥440
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圖片:
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IHC image of CSB-PA023891LA01HU diluted at 1:400 and staining in paraffin-embedded human prostate tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
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其他:
產(chǎn)品詳情
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產(chǎn)品名稱:Rabbit anti-Homo sapiens (Human) TMEM87B Polyclonal antibody
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Uniprot No.:
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基因名:TMEM87B
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別名:TMEM87B; Transmembrane protein 87B
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宿主:Rabbit
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反應(yīng)種屬:Human
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免疫原:Recombinant Human Transmembrane protein 87B protein (451-554AA)
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免疫原種屬:Homo sapiens (Human)
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標記方式:Non-conjugated
本頁面中的產(chǎn)品,TMEM87B Antibody (CSB-PA023891LA01HU),的標記方式是Non-conjugated。對于TMEM87B Antibody,我們還提供其他標記。見下表:
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克隆類型:Polyclonal
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抗體亞型:IgG
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純化方式:>95%, Protein G purified
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濃度:It differs from different batches. Please contact us to confirm it.
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保存緩沖液:Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, pH 7.4 -
產(chǎn)品提供形式:Liquid
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應(yīng)用范圍:ELISA, IHC
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推薦稀釋比:
Application Recommended Dilution IHC 1:200-1:500 -
Protocols:
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儲存條件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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貨期:Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
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用途:For Research Use Only. Not for use in diagnostic or therapeutic procedures.
相關(guān)產(chǎn)品
靶點詳情
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功能:May be involved in retrograde transport from endosomes to the trans-Golgi network (TGN).
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基因功能參考文獻:
- Heterozygous loss of FBLN7 and TMEM87B account for some of the clinical features, including cardiac defects and craniofacial abnormalities associated with 2q13 deletion syndrome. PMID: 24694933
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相關(guān)疾病:TMEM87B mutations may be involved in restrictive cardiomyopathy (RCM), a rare non-ischemic myocardial disease. RCM is characterized by restrictive ventricular-filling physiology in the presence of normal or reduced diastolic and/or systolic volumes (of 1 or both ventricles), biatrial enlargement, and normal ventricular wall thickness.
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亞細胞定位:Golgi apparatus membrane; Multi-pass membrane protein.
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蛋白家族:LU7TM family, TMEM87 subfamily
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數(shù)據(jù)庫鏈接:
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