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Alpha-1D Adrenergic Receptor A

ntibody[47948]
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  • 询价
  • Signalway Antibody已认证
  • 47948
  • 2025年09月23日
  • WB, IHC, IF/ICC
  • Rabbit
  • Human
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 免疫原

      KLH-conjugated synthetic peptide encompassing a sequence within the C-term region of human Alpha-1D Adrenergic Receptor.

    • 形态

      liquid

    • 保存条件

      Store at -20˚C

    • 克隆性

      Polyclonal

    • 适应物种

      Human

    • 保质期

      12 months

    • 抗原来源

      Rabbit

    • 供应商

      南京赛戈巍生物科技有限公司

    • 宿主

      Rabbit

    • 应用范围

      WB, IHC, IF/ICC

    • 靶点

      Uniprot:P25100

    • 抗体英文名

      Alpha-1D Adrenergic Receptor Antibody

    • 规格

      50ul/100ul

    别名:ADRA1A; Alpha-1D adrenergic receptor; Alpha-1A adrenergic receptor; Alpha-1D adrenoreceptor; Alpha-1D adrenoceptor; Alpha-adrenergic receptor 1a
    计算分子量:60KD
    配方:Liquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
    应用详情:

    Western blotting:1:500 - 1:1000
    Immunohistochemistry:1:50 - 1:100
    Immunofluorescence:1:100 - 1:300


    图片:

    产品细节图片1

    Western blot analysis of Alpha-1D Adrenergic Receptor expression in H9C2 (A), Raw264.7 (B), U87MG (C) whole cell lysates

    ,

    产品细节图片2

    Immunohistochemical analysis of Alpha-1D Adrenergic Receptor staining in human breast cancer formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.

    ,

    产品细节图片3

    Immunofluorescent analysis of Alpha-1D Adrenergic Receptor staining in MCF7 cells. Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with the primary antibody in 3% BSA-PBS and incubated overnight at 4 °C in a hidified chamber. Cells were washed with PBST and incubated with a DyLight 594-conjugated secondary antibody (red) in PBS at room temperature in the dark. DAPI was used to stain the cell nuclei (blue).


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    图标文献和实验
    相关实验
    • Isolation of Adrenergic Receptor Genes

      In order to isolate a single gene, phage or cosmid libraries can be screened by the conventional technique of hybridization as described by Sambrook et al. (1 ) using end-labeled oligonucleotide probes or gene-specific probes. The probes

    • Analyses of Adrenergic Receptor Sequences

      with known adrenergic receptor sequences in order to verify the receptor and subtype, to submit the sequence to GenBank, and to analyze the predicted secondary structure of the receptor.

    • Targeted Disruption of Adrenergic Receptor Genes

      . This approach has been particularly useful for studies on adrenergic receptor (AR) function, having been used to effect disruption of at least six of the nine known AR genes (1 –6 ). As presented here, the knockout strategy is essentially a synthesis

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