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CSRP3 抗体

CSRP3 适用: 人, 小鼠, 大鼠 IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7262435
发货至: 中国
  • 抗原 See all CSRP3 抗体
    CSRP3 (Cysteine and Glycine-Rich Protein 3 (CSRP3))
    适用
    • 39
    • 20
    • 9
    • 5
    • 4
    • 3
    • 3
    • 3
    • 1
    • 1
    • 1
    人, 小鼠, 大鼠
    宿主
    • 36
    • 2
    • 1
    克隆类型
    • 37
    • 2
    多克隆
    标记
    • 22
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This CSRP3 antibody is un-conjugated
    应用范围
    • 30
    • 22
    • 7
    • 7
    • 2
    • 1
    • 1
    • 1
    • 1
    Immunohistochemistry (IHC)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein of human CSRP3 (NP_003467.1).
    亚型
    IgG
  • 应用备注
    IHC 1:50-1:200
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 mg/mL
    缓冲液
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    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
    -20 °C
    储存方法
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    CSRP3 (Cysteine and Glycine-Rich Protein 3 (CSRP3))
    别名
    CSRP3 (CSRP3 产品)
    别名
    CLP antibody, CMD1M antibody, CMH12 antibody, CRP3 antibody, LMO4 antibody, MLP antibody, MMLP antibody, csrp3 antibody, zgc:103468 antibody, CSRP3 antibody, csrp3-a antibody, cysteine and glycine rich protein 3 antibody, cysteine and glycine-rich protein 3 antibody, cysteine and glycine-rich protein 3 (cardiac LIM protein) antibody, cysteine and glycine rich protein 3 L homeolog antibody, CSRP3 antibody, Csrp3 antibody, csrp3 antibody, csrp3.L antibody
    背景
    This gene encodes a member of the CSRP family of LIM domain proteins, which may be involved in regulatory processes important for development and cellular differentiation. The LIM/double zinc-finger motif found in this protein is found in a group of proteins with critical functions in gene regulation, cell growth, and somatic differentiation. Mutations in this gene are thought to cause heritable forms of hypertrophic cardiomyopathy (HCM) and dilated cardiomyopathy (DCM) in humans. Alternatively spliced transcript variants with different 5' UTR, but encoding the same protein, have been found for this gene.
    基因ID
    8048
    UniProt
    P50461
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