TMEM87B Antibody, HRP conjugated
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中文名稱：TMEM87B兔多克隆抗體, HRP偶聯(lián)
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貨號(hào)：CSB-PA023891LB01HU
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規(guī)格：￥880
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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(biāo)記方式：HRP
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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
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Protocols：
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儲(chǔ)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.
產(chǎn)品評(píng)價(jià)
相關(guān)產(chǎn)品
靶點(diǎn)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(xiàn)：
- 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(xì)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(kù)鏈接：
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