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SVOPL 抗体 (Middle Region)

SVOPL 适用: 人 WB, EIA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN955017
发货至: 中国
  • 抗原 See all SVOPL products
    SVOPL (SVOP-Like (SVOPL))
    抗原表位
    • 7
    • 6
    • 6
    • 6
    • 6
    • 1
    AA 240-269, Middle Region
    适用
    • 21
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    宿主
    • 21
    克隆类型
    • 21
    多克隆
    标记
    • 7
    • 4
    • 3
    • 3
    • 2
    • 2
    This SVOPL antibody is un-conjugated
    应用范围
    • 17
    • 16
    • 1
    • 1
    • 1
    Western Blotting (WB), Enzyme Immunoassay (EIA)
    特异性
    This antibody detects SVOPL (Center).
    交叉反应 (详细)
    Species reactivity (tested):Human
    纯化方法
    Protein A column followed by peptide affinity purification
    免疫原
    KLH conjugated synthetic peptide between 240-269 amino acids from the Central region of human SVOPL
    亚型
    Ig Fraction
  • 应用备注
    Optimal working dilution should be determined by the investigator.
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.25 mg/mL
    缓冲液
    PBS, 0.09 % (W/V) sodium azide
    储存液
    Sodium azide
    注意事项
    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    注意事项
    Avoid repeated freezing and thawing.
    储存条件
    4 °C/-20 °C
    储存方法
    Store at 2 - 8 °C for up to six months or (in aliquots) at -20 °C for longer.
  • 抗原
    SVOPL (SVOP-Like (SVOPL))
    别名
    SVOPL (SVOPL 产品)
    别名
    zgc:101741 antibody, 9430071P14Rik antibody, SVOP like antibody, SVOP-like antibody, SV2 related protein homolog (rat)-like antibody, SVOPL antibody, svopl antibody, Svopl antibody
    背景
    SVOPL (putative transporter SVOPL), also known as SV2-related protein-like, is a 492 amino acid multi-pass membrane protein belonging to the major facilitator superfamily. SVOPL is a paralog to synaptic vesicle protein (SVOP) that exists as two alternatively spliced isoforms. The gene encoding SVOPL maps to human chromosome 7q34. Chromosome 7 is approximately 158 milllion bases long, encodes over 1,000 genes and makes up approximately 5 % of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. Deletions of portions of the q arm of chromosome 7 are linked to myeloid disorders, including acute myelogenous leukemia and myelodysplasia.Synonyms: Putative transporter
    分子量
    Molecular Weight: 53991 Da
    基因ID
    136306
    NCBI登录号
    NP_001132928
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