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Chordin 抗体

CHRD 适用: 人, 小鼠, 大鼠 IHC, ELISA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7246175
发货至: 中国
  • 抗原 See all Chordin (CHRD) 抗体
    Chordin (CHRD)
    适用
    人, 小鼠, 大鼠
    宿主
    • 55
    • 1
    克隆类型
    • 55
    • 1
    多克隆
    标记
    • 18
    • 7
    • 5
    • 5
    • 5
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    This Chordin antibody is un-conjugated
    应用范围
    • 35
    • 32
    • 21
    • 5
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    Immunohistochemistry (IHC), ELISA
    产品特性
    Polyclonal Antibody
    纯化方法
    Antigen affinity purification
    免疫原
    Fusion protein of human CHRD
    亚型
    IgG
    Top Product
    Discover our top product CHRD Primary Antibody
  • 应用备注
    IHC 1:30-1:150, ELISA 1:5000-1:10000
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.8 mg/mL
    缓冲液
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    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
    Chordin (CHRD)
    别名
    CHRD (CHRD 产品)
    别名
    chd antibody, X-chordin antibody, Chd antibody, chordino antibody, wu:fe47d04 antibody, chordin antibody, chordin, gene 1 antibody, chordin, gene 1 S homeolog antibody, CHRD antibody, chrd.1 antibody, LOC778563 antibody, Chrd antibody, chrd antibody, chrd.1.S antibody
    背景
    CHRD (Chordin) is a Protein Coding gene. Diseases associated with CHRD include Cornelia De Lange Syndrome. Among its related pathways are Mesodermal Commitment Pathway and TGF-beta signaling pathway (KEGG). GO annotations related to this gene include heparin binding and syndecan binding. An important paralog of this gene is CHRDL2.This gene encodes a secreted protein that dorsalizes early vertebrate embryonic tissues by binding to ventralizing TGF-beta-like bone morphogenetic proteins and sequestering them in latent complexes. The encoded protein may also have roles in organogenesis and during adulthood. It has been suggested that this gene could be a candidate gene for Cornelia de Lange syndrome. Reduced expression of this gene results in enhanced bone regeneration. Alternative splicing results in multiple transcript variants. Other alternative splice variants have been described but their full length sequence has not been determined.
    UniProt
    Q9H2X0
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