RAB40AL Antibody, Biotin conjugated
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中文名稱:
RAB40AL兔多克隆抗體, Biotin偶聯
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貨號:
CSB-PA019203LD01HU
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規格:
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其他:
產品詳情
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產品名稱:
Rabbit anti-Homo sapiens (Human) RAB40AL Polyclonal antibody
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Uniprot No.:
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基因名:
RAB40AL
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別名:
RAB40AL antibody; RLGP antibody; Ras-related protein Rab-40A-like antibody; Ras-like GTPase antibody
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宿主:
Rabbit
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反應種屬:
Human
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免疫原:
Recombinant Human Ras-related protein Rab-40A-like protein (1-88AA)
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免疫原種屬:
Homo sapiens (Human)
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標記方式:
Biotin
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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
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產品提供形式:
Liquid
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應用范圍:
ELISA
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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.
靶點詳情
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功能:
May be a substrate-recognition component of a SCF-like ECS (Elongin-Cullin-SOCS-box protein) E3 ubiquitin ligase complex which mediates the ubiquitination and subsequent proteasomal degradation of target proteins.
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基因功能參考文獻:
- Our findings are inconsistent with a causative effect of RAB40AL p.D59G on cognitive impairment combined with severe to profound bilateral hearing loss but indicate that p.D59G is a common genetic variation. PMID: 25370018
- Data question the role of RAB40AL mutation as a disease-causing change and the involvement of RAB40AL in Martin-Probst syndrome. PMID: 25044830
- We herein present an unrelated 20-year-old male with similar manifestations also with p.D59G in the RAB40AL gene, which supports the existence of this condition previously coined as Martin-Probst syndrome PMID: 24863632
- This is the first study to show that mutation of RAB40AL is associated with a human disorder. PMID: 22581972
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相關疾病:
Mental retardation, X-linked, syndromic, Martin-Probst type (MRXSMP)
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亞細胞定位:
Membrane; Lipid-anchor; Cytoplasmic side. Cytoplasm. Mitochondrion.
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蛋白家族:
Small GTPase superfamily, Rab family
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組織特異性:
Expressed in brain, lung, heart, skeletal muscle, kidney and liver. Highest expression in brain. Expressed in fetal brain and kidney.
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數據庫鏈接:
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