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SLC39A5 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

SLC39A5 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 ABIN2735909
发货至: 中国
  • 抗原 See all SLC39A5 蛋白
    SLC39A5 (Solute Carrier Family 39 (Metal Ion Transporter), Member 5 (SLC39A5))
    蛋白类型
    Recombinant
    产品特性
    Transcript Variant 1
    宿主
    • 4
    • 3
    资源
    • 4
    • 2
    • 1
    HEK-293 Cells
    标记
    This SLC39A5 protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human Zinc transporter ZIP5 / SLC39A5 (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 SLC39A5 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
    SLC39A5 (Solute Carrier Family 39 (Metal Ion Transporter), Member 5 (SLC39A5))
    别名
    Zinc Transporter Zip5,slc39a5 (SLC39A5 产品)
    别名
    1810013D05Rik Protein, 2010205A06Rik Protein, Zip5 Protein, LZT-Hs7 Protein, ZIP5 Protein, solute carrier family 39 member 5 Protein, solute carrier family 39 (metal ion transporter), member 5 Protein, SLC39A5 Protein, Slc39a5 Protein
    背景
    The protein encoded by this gene belongs to the ZIP family of zinc transporters that transport zinc into cells from outside, and play a crucial role in controlling intracellular zinc levels. Zinc is an essential cofactor for many enzymes and proteins involved in gene transcription, growth, development and differentiation. Mutations in this gene have been associated with autosomal dominant high myopia (MYP24). Alternatively spliced transcript variants have been found for this gene.
    分子量
    56.1 kDa
    NCBI登录号
    NP_775867
    途径
    Transition Metal Ion Homeostasis
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