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Distal-Less Homeobox 5 (DLX5) Peptide

DLX5 适用: 人 宿主: 合成 BP, IHC, WB
产品编号 ABIN975853
发货至: 中国
  • 抗原 See all DLX5 products
    DLX5 (Distal-Less Homeobox 5 (DLX5))
    宿主
    资源
    • 6
    合成
    应用范围
    Blocking Peptide (BP), Immunohistochemistry (IHC), Western Blotting (WB)
    产品特性
    This is a synthetic peptide designed for use in combination with anti-DLX5 antibody (Catalog #: ARP32867_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
    纯化方法
    Purified
  • 应用备注
    Each Investigator should determine their own optimal working dilution for specific applications.
    限制
    仅限研究用
  • 状态
    Lyophilized
    溶解方式
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    浓度
    1 mg/mL
    缓冲液
    Final peptide concentration is 1 mg/mL in PBS.
    注意事项
    Avoid repeated freeze-thaw cycles.
    储存条件
    -20 °C
    储存方法
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • 抗原
    DLX5 (Distal-Less Homeobox 5 (DLX5))
    别名
    SHFM1D Peptide, AI385752 Peptide, RDLX Peptide, X-dll3 Peptide, dll3 Peptide, MGC69418 Peptide, DLX5 Peptide, dlx5 Peptide, dlx4 Peptide, zgc:101787 Peptide, distal-less homeobox 5 Peptide, distal-less homeobox 5 L homeolog Peptide, distal-less homeobox 2b Peptide, distal-less homeobox 5a Peptide, DLX5 Peptide, Dlx5 Peptide, dlx5.L Peptide, dlx5 Peptide, dlx2b Peptide, dlx5a Peptide
    背景
    DLX5 is a member of a homeobox transcription factor family. DLX5 may play a role in bone development and fracture healing. Mutation in this gene, which is located in a tail-to-tail configuration with another member of the family on the long arm of chromosome 7, may be associated with split-hand/split-foot malformation.This gene encodes a member of a homeobox transcription factor gene family similiar to the Drosophila distal-less gene. The encoded protein may play a role in bone development and fracture healing. Mutation in this gene, which is located in a tail-to-tail configuration with another member of the family on the long arm of chromosome 7, may be associated with split-hand/split-foot malformation.This gene encodes a member of a homeobox transcription factor gene family similiar to the Drosophila distal-less gene. The encoded protein may play a role in bone development and fracture healing. Mutation in this gene, which is located in a tail-to-tail configuration with another member of the family on the long arm of chromosome 7, may be associated with split-hand/split-foot malformation.

    Alias Symbols: SHFM1D

    Protein Interaction Partner: MAGED1,MSX2,NCOA2,SOX10,SOX8,SPEN,DLX2,DLX5,HOXC8,MSX1,MSX2

    Protein Size: 289
    分子量
    31 kDa
    基因ID
    1749
    NCBI登录号
    NM_005221, NP_005212
    UniProt
    P56178
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