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DGCR6L 抗体

This 兔 多克隆 antibody specifically detects DGCR6L in WB, ICC 和 IF. It exhibits reactivity toward 人.
产品编号 ABIN7466886
发货至: 中国
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Quick Overview for DGCR6L 抗体 (ABIN7466886)

抗原

See all DGCR6L 抗体
DGCR6L (DiGeorge Syndrome Critical Region Gene 6-Like (DGCR6L))

适用

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宿主

  • 40
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克隆类型

  • 41
多克隆

标记

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This DGCR6L antibody is un-conjugated

应用范围

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Western Blotting (WB), Immunocytochemistry (ICC), Immunofluorescence (IF)
  • 交叉反应

    人, 小鼠

    纯化方法

    Purified by antigen-affinity chromatography.

    免疫原

    Recombinant protein encompassing a sequence within the center region of human DGCR6L. The exact sequence is proprietary.

    亚型

    IgG
  • 应用备注

    WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    说明

    Positive Control: mouse liver

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    0.76 mg/mL

    缓冲液

    0.1M Tris-Glycine ( pH 7), 20 % Glycerol, 0.01 % Thimerosal

    储存液

    Thimerosal (Merthiolate)

    注意事项

    This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    储存条件

    4 °C,-20 °C

    储存方法

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • 抗原

    DGCR6L (DiGeorge Syndrome Critical Region Gene 6-Like (DGCR6L))

    别名

    DiGeorge syndrome critical region gene 6 like

    背景

    DiGeorge syndrome critical region gene 6 like , DGCR6,This gene, the result of a duplication at this locus, is one of two functional genes encoding nearly identical proteins that have similar expression patterns. The product of this gene is a protein that shares homology with the Drosophila gonadal protein, expressed in gonadal tissues and germ cells, and with the human laminin gamma-1 chain that functions in cell attachment and migration. This gene is located in a region of chromosome 22 implicated in the DiGeorge syndrome, one facet of a broader collection of anomalies referred to as the CATCH 22 syndrome. [provided by RefSeq]

    分子量

    25 kDa

    基因ID

    85359

    UniProt

    Q9BY27
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