RBM28 Antibody
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中文名稱：RBM28兔多克隆抗體
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貨號：CSB-PA019419GA01HU
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規格：￥3,900
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其他：
產品詳情
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Uniprot No.：
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基因名：
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別名：2810480G15Rik antibody; FLJ10377 antibody; RBM 28 antibody; RBM28 antibody; RBM28_HUMAN antibody; RNA binding motif protein 28 antibody; RNA binding protein 28 antibody; RNA-binding motif protein 28 antibody; RNA-binding protein 28 antibody
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宿主：Rabbit
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反應種屬：Human,Mouse,Rat
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免疫原：Human RBM28
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免疫原種屬：Homo sapiens (Human)
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抗體亞型：IgG
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純化方式：Antigen Affinity 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：PBS with 0.1% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
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產品提供形式：Liquid
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應用范圍：ELISA,WB
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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.
產品評價
相關產品
靶點詳情
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功能：Nucleolar component of the spliceosomal ribonucleoprotein complexes.
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基因功能參考文獻：
- The authors conclude that the ANE syndrome mutation generates defective RBM28 protein folding which abrogates protein-protein interactions and causes faulty pre-large subunit rRNA processing, thus revealing one aspect of the molecular basis of this human disease. PMID: 27077951
- RBM28 controls the expression of miR-203. RBM28 contributes to hair follicle growth regulation through modulation of miR-203 and p63 activity. PMID: 25939713
- RBM28 gene defects should be added to the growing list of gene defects associated with syndromic combined anterior pituitary hormone deficiency. PMID: 20231366
- RBM28 is a common nucleolar component of the spliceosomal ribonucleoprotein complexes, possibly coordinating their transition through the nucleolus PMID: 17081119
- A loss-of-function mutation is found in RBM28, encoding a nucleolar protein in patients with alopecia, progressive neurological defects, and endocrinopathy (ANE syndrome). PMID: 18439547
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相關疾病：Alopecia, neurologic defects, and endocrinopathy syndrome (ANES)
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亞細胞定位：Nucleus, nucleolus.
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組織特異性：Ubiquitously expressed.
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數據庫鏈接：
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