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ROR2 抗体

ROR2 适用: 人, 小鼠, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7261561
发货至: 中国
  • 抗原 See all ROR2 抗体
    ROR2 (Receptor Tyrosine Kinase-Like Orphan Receptor 2 (ROR2))
    适用
    • 69
    • 27
    • 22
    • 1
    • 1
    • 1
    • 1
    人, 小鼠, 大鼠
    宿主
    • 63
    • 9
    克隆类型
    • 61
    • 11
    多克隆
    标记
    • 38
    • 5
    • 5
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    This ROR2 antibody is un-conjugated
    应用范围
    • 46
    • 28
    • 26
    • 12
    • 7
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    A synthetic peptide of human ROR2 (NP_004551.2).
    亚型
    IgG
    Top Product
    Discover our top product ROR2 Primary Antibody
  • 应用备注
    WB 1:500-1:2000
    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
    ROR2 (Receptor Tyrosine Kinase-Like Orphan Receptor 2 (ROR2))
    别名
    ROR2 (ROR2 产品)
    别名
    BDB antibody, BDB1 antibody, NTRKR2 antibody, Ntrkr2 antibody, mRor2 antibody, ROR2 antibody, bdb antibody, bdb1 antibody, Xror2 antibody, ntrkr2 antibody, MGC97773 antibody, LOC100219935 antibody, ror2 antibody, xror2 antibody, receptor tyrosine kinase like orphan receptor 2 antibody, receptor tyrosine kinase-like orphan receptor 2 antibody, receptor tyrosine kinase like orphan receptor 2 L homeolog antibody, ROR2 antibody, Ror2 antibody, ror2 antibody, ror2.L antibody
    背景
    The protein encoded by this gene is a receptor protein tyrosine kinase and type I transmembrane protein that belongs to the ROR subfamily of cell surface receptors. The protein may be involved in the early formation of the chondrocytes and may be required for cartilage and growth plate development. Mutations in this gene can cause brachydactyly type B, a skeletal disorder characterized by hypoplasia/aplasia of distal phalanges and nails. In addition, mutations in this gene can cause the autosomal recessive form of Robinow syndrome, which is characterized by skeletal dysplasia with generalized limb bone shortening, segmental defects of the spine, brachydactyly, and a dysmorphic facial appearance.
    分子量

    Observed_MW: 135 kDa

    Calculated_MW: 104 kDa

    基因ID
    4920
    UniProt
    Q01974
    途径
    RTK signaling, WNT signaling
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