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DYNC2H1 抗体

DYNC2H1 适用: 大鼠 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN6567791
发货至: 中国
  • 抗原 See all DYNC2H1 抗体
    DYNC2H1 (Dynein, Cytoplasmic 2, Heavy Chain 1 (DYNC2H1))
    适用
    • 15
    • 3
    • 1
    大鼠
    宿主
    • 15
    克隆类型
    • 15
    多克隆
    标记
    • 6
    • 3
    • 2
    • 2
    • 1
    • 1
    This DYNC2H1 antibody is un-conjugated
    应用范围
    • 11
    • 10
    • 1
    • 1
    Western Blotting (WB)
    纯化方法
    Affinity purification
    免疫原
    Recombinant Protein of human DYNC2H1
    亚型
    IgG
    Top Product
    Discover our top product DYNC2H1 Primary Antibody
  • 应用备注
    WB 1:500 - 1:2000
    限制
    仅限研究用
  • 浓度
    1 mg/mL
    缓冲液
    Buffer: 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
    DYNC2H1 (Dynein, Cytoplasmic 2, Heavy Chain 1 (DYNC2H1))
    别名
    DYNC2H1 (DYNC2H1 产品)
    别名
    dhc2 antibody, dhc1b antibody, dnch2 antibody, dyh1b antibody, 4432416O06Rik antibody, AI448217 antibody, D030010H02Rik antibody, D330044F14Rik antibody, DHC1b antibody, DHC2 antibody, Dnchc2 antibody, b2b414Clo antibody, mKIAA1997 antibody, Dnch2 antibody, ATD3 antibody, DNCH2 antibody, DYH1B antibody, SRPS2B antibody, hdhc11 antibody, dynein cytoplasmic 2 heavy chain 1 antibody, dynein, cytoplasmic 2, heavy chain 1 antibody, cytoplasmic dynein 1b heavy chain antibody, DYNC2H1 antibody, dync2h1 antibody, DHC1b antibody, Dync2h1 antibody
    背景

    Synonyms: Cytoplasmic dynein 2 heavy chain 1,Cytoplasmic dynein 2 heavy chain,DYHC2,DYNC2H1,Dynein cytoplasmic heavy chain 2,Dynein heavy chain 11,Dynein heavy chain isotype 1B,hDHC11

    Background: This gene encodes a large cytoplasmic dynein protein that is involved in retrograde transport in the cilium and has a role in intraflagellar transport, a process required for ciliary/flagellar assembly. Mutations in this gene cause a heterogeneous spectrum of conditions related to altered primary cilium function and often involve polydactyly, abnormal skeletogenesis, and polycystic kidneys. Alternative splicing results in multiple transcript variants encoding distinct proteins.

    分子量

    Observed_MW: 493kDa

    Calculated_MW: 105kDa/492kDa/493kDa

    基因ID
    79659
    UniProt
    Q8NCM8
    途径
    Hedgehog Signaling, Asymmetric Protein Localization
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