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IFT43 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

IFT43 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 ABIN2714061
发货至: 中国
  • 抗原 See all IFT43 蛋白
    IFT43 (Intraflagellar Transport 43 Homolog (IFT43))
    蛋白类型
    Recombinant
    产品特性
    Transcript Variant 1
    宿主
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    资源
    • 6
    • 2
    HEK-293 Cells
    标记
    This IFT43 protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human Chromosome 14 open reading frame 179 (C14orf179), transcript variant 1 (transcript variant 1) 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 IFT43 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
    IFT43 (Intraflagellar Transport 43 Homolog (IFT43))
    别名
    Chromosome 14 Open Reading Frame 179 (c14orf179) (IFT43 产品)
    别名
    C10H14orf179 Protein, C14orf179 Protein, CED3 Protein, 1700019E19Rik Protein, R75064 Protein, c14orf179 Protein, RGD1307392 Protein, intraflagellar transport 43 Protein, intraflagellar transport 43 L homeolog Protein, intraflagellar transport 43 homolog (Chlamydomonas) Protein, IFT43 Protein, Ift43 Protein, ift43.L Protein
    背景
    This gene encodes a subunit of the intraflagellar transport complex A (IFT-A). IFT-A is a multiprotein complex that plays an important role in cilia assembly and maintenance by mediating retrograde ciliary transport. Mutations in this gene are a cause of cranioectodermal dysplasia-3 (CED3), also known as Sensenbrenner syndrome. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene.
    分子量
    23.7 kDa
    NCBI登录号
    NP_443105
    途径
    Hedgehog Signaling
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