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SGCA 抗体 (AA 239-266)

SGCA 适用: 人 WB 宿主: 兔 Polyclonal RB36903 unconjugated
产品编号 ABIN1538155
发货至: 中国
  • 抗原 See all SGCA 抗体
    SGCA (Sarcoglycan, alpha (50kDa Dystrophin-Associated Glycoprotein) (SGCA))
    抗原表位
    • 10
    • 7
    • 6
    • 6
    • 5
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 239-266
    适用
    • 46
    • 21
    • 18
    • 1
    • 1
    宿主
    • 47
    • 3
    克隆类型
    • 38
    • 12
    多克隆
    标记
    • 21
    • 5
    • 4
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    This SGCA antibody is un-conjugated
    应用范围
    • 32
    • 23
    • 4
    • 4
    • 3
    • 2
    • 1
    • 1
    Western Blotting (WB)
    纯化方法
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    免疫原
    This SGCA antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 239-266 amino acids from the Central region of human SGCA.
    克隆位点
    RB36903
    亚型
    Ig Fraction
    Top Product
    Discover our top product SGCA Primary Antibody
  • 应用备注
    WB: 1:1000
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    Purified polyclonal antibody supplied in PBS with 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.
    储存条件
    4 °C,-20 °C
    储存方法
    SGCA Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.
    有效期
    6 months
  • 抗原
    SGCA (Sarcoglycan, alpha (50kDa Dystrophin-Associated Glycoprotein) (SGCA))
    别名
    SGCA (SGCA 产品)
    别名
    Sgca antibody, 50-DAG antibody, A2 antibody, ADL antibody, DAG2 antibody, DMDA2 antibody, LGMD2D antibody, SCARMD1 antibody, adhalin antibody, 50DAG antibody, Asg antibody, sarcoglycan alpha antibody, sarcoglycan, alpha (dystrophin-associated glycoprotein) antibody, sarcoglycan, alpha antibody, SGCA antibody, Sgca antibody
    背景
    This gene encodes a component of the dystrophin-glycoprotein complex (DGC), which is critical to the stability of muscle fiber membranes and to the linking of the actin cytoskeleton to the extracellular matrix. Its expression is thought to be restricted to striated muscle. Mutations in this gene result in type 2D autosomal recessive limb-girdle muscular dystrophy. Multiple transcript variants encoding different isoforms have been found for this gene.
    分子量
    42875
    基因ID
    6442
    NCBI登录号
    NP_000014, NP_001129169
    UniProt
    Q16586
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