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NK2 Homeobox 5 抗体

NKX2-5 适用: 小鼠, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN6293408
发货至: 中国
  • 抗原 See all NK2 Homeobox 5 (NKX2-5) 抗体
    NK2 Homeobox 5 (NKX2-5)
    适用
    • 41
    • 20
    • 7
    • 5
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    小鼠, 大鼠
    宿主
    • 43
    • 7
    • 1
    克隆类型
    • 45
    • 6
    多克隆
    标记
    • 37
    • 4
    • 3
    • 3
    • 2
    • 2
    This NK2 Homeobox 5 antibody is un-conjugated
    应用范围
    • 44
    • 30
    • 5
    • 5
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB)
    纯化方法
    Affinity purification
    免疫原
    A synthetic peptide of human NKX2-5
    亚型
    IgG
    Top Product
    Discover our top product NKX2-5 Primary Antibody
  • 应用备注
    WB 1:500 - 1:2000
    说明

    Expressed only in the heart

    限制
    仅限研究用
  • 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 -20C. Avoid freeze / thaw cycles.
  • 抗原
    NK2 Homeobox 5 (NKX2-5)
    别名
    NKX2-5 (NKX2-5 产品)
    别名
    CHNG5 antibody, CSX antibody, CSX1 antibody, HLHS2 antibody, NKX2.5 antibody, NKX2E antibody, NKX4-1 antibody, VSD3 antibody, Csx antibody, Nkx-2.5 antibody, Nkx2.5 antibody, tinman antibody, nk2.5 antibody, nkx2-5 antibody, zgc:111912 antibody, AR2 antibody, XNkx2-5 antibody, csx antibody, nkx-2.5 antibody, nkx2-5b antibody, nkx2.5 antibody, NKX2-5 antibody, Nkx2-5 antibody, csx1 antibody, nkx2e antibody, XNkx-2.5 antibody, CNKX-2.5 antibody, NKX-2.5 antibody, NK2 homeobox 5 antibody, NK2 homeobox 5 S homeolog antibody, NKX2-5 antibody, Nkx2-5 antibody, nkx2.5 antibody, nkx2-5.S antibody, nkx2-5 antibody
    背景
    This gene encodes a homeobox-containing transcription factor. This transcription factor functions in heart formation and development. Mutations in this gene cause atrial septal defect with atrioventricular conduction defect, and also tetralogy of Fallot, which are both heart malformation diseases. Mutations in this gene can also cause congenital hypothyroidism non-goitrous type 5, a non-autoimmune condition. Alternative splicing results in multiple transcript variants.
    分子量
    34.918 kDa
    基因ID
    1482
    UniProt
    P52952
    途径
    Regulation of Muscle Cell Differentiation, Skeletal Muscle Fiber Development
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