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COMP 抗体

COMP 适用: 人, 小鼠, 大鼠 WB, IHC, ELISA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7236649
发货至: 中国
  • 抗原 See all COMP 抗体
    COMP (Cartilage Oligomeric Matrix Protein (COMP))
    适用
    • 56
    • 31
    • 24
    • 1
    • 1
    • 1
    • 1
    • 1
    人, 小鼠, 大鼠
    宿主
    • 70
    • 7
    • 1
    克隆类型
    • 72
    • 6
    多克隆
    标记
    • 28
    • 12
    • 7
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This COMP antibody is un-conjugated
    应用范围
    • 71
    • 24
    • 19
    • 18
    • 13
    • 9
    • 9
    • 6
    • 5
    • 4
    • 4
    • 3
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC), ELISA
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant protein of human COMP
    亚型
    IgG
    Top Product
    Discover our top product COMP Primary Antibody
  • 应用备注
    WB 1:500-1:2000, IHC 1:50-1:200
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.3 mg/mL
    缓冲液
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    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
    COMP (Cartilage Oligomeric Matrix Protein (COMP))
    别名
    COMP (COMP 产品)
    别名
    COMP antibody, EDM1 antibody, EPD1 antibody, MED antibody, PSACH antibody, THBS5 antibody, TSP5 antibody, cartilage oligomeric matrix protein antibody, COMP antibody, sce3551 antibody, CJA_1292 antibody, Comp antibody
    背景
    The protein encoded by this gene is a noncollagenous extracellular matrix (ECM) protein. It consists of five identical glycoprotein subunits, each with EGF-like and calcium-binding (thrombospondin-like) domains. Oligomerization results from formation of a five-stranded coiled coil and disulfides. Binding to other ECM proteins such as collagen appears to depend on divalent cations. Mutations can cause the osteochondrodysplasias pseudochondroplasia (PSACH) and multiple epiphyseal dysplasia (MED).
    分子量
    83 kDa
    UniProt
    P49747
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