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NK2 Homeobox 5 Protein (NKX2-5) (Myc-DYKDDDDK Tag)

NKX2-5 宿主: 人 宿主: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
产品编号 ABIN2727353
发货至: 中国
  • 抗原 See all NK2 Homeobox 5 (NKX2-5) 蛋白
    NK2 Homeobox 5 (NKX2-5)
    蛋白类型
    Recombinant
    宿主
    • 2
    • 1
    • 1
    • 1
    • 1
    资源
    • 3
    • 2
    • 1
    HEK-293 Cells
    标记
    This NK2 Homeobox 5 protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human NKX2-5 protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    纯度
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product NKX2-5 蛋白
  • 应用备注
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    说明

    The tag is located at the C-terminal.

    限制
    仅限研究用
  • 浓度
    50 μg/mL
    缓冲液
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    储存条件
    -80 °C
    储存方法
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • 抗原
    NK2 Homeobox 5 (NKX2-5)
    别名
    Nkx2-5 (NKX2-5 产品)
    别名
    CHNG5 Protein, CSX Protein, CSX1 Protein, HLHS2 Protein, NKX2.5 Protein, NKX2E Protein, NKX4-1 Protein, VSD3 Protein, Csx Protein, Nkx-2.5 Protein, Nkx2.5 Protein, tinman Protein, nk2.5 Protein, nkx2-5 Protein, zgc:111912 Protein, AR2 Protein, XNkx2-5 Protein, csx Protein, nkx-2.5 Protein, nkx2-5b Protein, nkx2.5 Protein, NKX2-5 Protein, Nkx2-5 Protein, csx1 Protein, nkx2e Protein, XNkx-2.5 Protein, CNKX-2.5 Protein, NKX-2.5 Protein, NK2 homeobox 5 Protein, NK2 homeobox 5 S homeolog Protein, NKX2-5 Protein, Nkx2-5 Protein, nkx2.5 Protein, nkx2-5.S Protein, nkx2-5 Protein
    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
    34.7 kDa
    NCBI登录号
    NP_004378
    途径
    Regulation of Muscle Cell Differentiation, Skeletal Muscle Fiber Development
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