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CQA2432
  • Western blot analysis of TPD52 expression in MCF7 (A), Hela (B), HT29 (C) whole cell lysates. (Predicted band size: 16; 19; 22; 24; 25; 26 kD; Observed band size: 26 kD)
  • Immunohistochemical analysis of TPD52 staining in human tonsil 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.
产品名称:Anti-TPD52 Antibody
货号:CQA2432
来源:Rabbit
反应物种:H
实验应用:WB, IH
*反应物种注解:
H - Human, M - Mouse, R - Rat, B - Bovine, C - Chicken, D - Dog, G - Goat, Mk - Monkey, P - Pig, Rb - Rabbit, S - Sheep, Z - Zebrafish
*实验应用注解:
E- ELISA, WB - Western blot, IH - Immunohistochemistry, IF - Immunofluorescence, FC - Flow cytometry, IC - Immunocytochemistry, IP - Immunoprecipitation, ChIP - Chromatin Immunoprecipitation, EMSA - Electrophoretic Mobility Shift Assay, BL - Blocking, SE - Sandwich ELISA, CBE - Cell-based ELISA, RNAi - RNA interference
规格
价格(元)
200 μl
3500
100 μl
2200
50 μl
1500
30 μl
1100
Ship in 3 days
产品描述:Rabbit polyclonal antibody to TPD52
免疫原:Recombinant full length protein of human TPD52
纯化方式:The antibody was purified by immunogen affinity chromatography.
克隆类型:Polyclonal
产品形式:Liquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
稀释比:WB (1/500 - 1/2000), IH (1/50 - 1/200)
基因名称:TPD52
相关名称:Tumor protein D52; Protein N8
基因编号(人): 7163;
蛋白编号(人): P55327;
储存效期:Shipped at 4°C. Upon delivery aliquot and store at -20°C for one year. Avoid freeze/thaw cycles.
  • Western blot analysis of TPD52 expression in MCF7 (A), Hela (B), HT29 (C) whole cell lysates. (Predicted band size: 16; 19; 22; 24; 25; 26 kD; Observed band size: 26 kD)
  • Immunohistochemical analysis of TPD52 staining in human tonsil 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.
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