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DiGeorge Syndrome Critical Region Gene 8 (DGCR8) (N-Term) Peptide

DGCR8 适用: 人 宿主: 合成 BP, WB, IHC
产品编号 ABIN975746
发货至: 中国
  • 抗原 See all DGCR8 products
    DGCR8 (DiGeorge Syndrome Critical Region Gene 8 (DGCR8))
    蛋白结构域
    N-Term
    宿主
    资源
    • 4
    合成
    应用范围
    Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
    产品特性
    This is a synthetic peptide designed for use in combination with anti-DGCR8 antibody (Catalog #: ARP40984_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
    DGCR8 (DiGeorge Syndrome Critical Region Gene 8 (DGCR8))
    别名
    MGC78846 Peptide, DGCR8 Peptide, gy1 Peptide, dgcrk6 Peptide, C22orf12 Peptide, DGCRK6 Peptide, Gy1 Peptide, pasha Peptide, D16H22S1742E Peptide, D16H22S788E Peptide, D16Wis2 Peptide, N41 Peptide, Vo59c07 Peptide, si:ch211-106a19.4 Peptide, wu:fc23f08 Peptide, wu:fc38f06 Peptide, DGCR8 microprocessor complex subunit L homeolog Peptide, DiGeorge syndrome critical region gene 8 Peptide, DGCR8 microprocessor complex subunit Peptide, DGCR8, microprocessor complex subunit Peptide, microRNA 3618 Peptide, dgcr8.L Peptide, DGCR8 Peptide, dgcr8 Peptide, Dgcr8 Peptide, MIR3618 Peptide
    背景
    DGCR8 contains 2 DRBM (double-stranded RNA-binding) domains and 1 WW domain. It may play a part in the etiology of the velocardiofacial/DiGeorge syndrome (VCFS/DGS), a developmental disorder characterized by structural and functional palate anomalies, conotruncal cardiac malformations, immunodeficiency, hypocalcemia, and typical facial anomalies.

    Alias Symbols: C22orf12, DGCRK6, Gy1, pasha

    Protein Interaction Partner: RNASEN,RNASEN,RNASEN

    Protein Size: 773
    分子量
    85 kDa
    基因ID
    54487
    NCBI登录号
    NM_022720, NP_073557
    UniProt
    Q8WYQ5
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