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CMA1199
  • Western blot analysis of BCL2 expression in H1792 (A), A2780 (B), HUT78 (C), mouse spleen (D), mouse kidney (E), rat spleen (F), rat kidney (G) whole cell lysates. (Predicted band size: 26 kD; Observed band size: 26 kD)
  • Immunohistochemical analysis of BCL2 staining in human stomach 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. Tyramide-AF488 (green) was used as the chromogen. The section was then counterstained with DAPI (blue).
  • Immunofluorescent analysis of BCL2 staining in HepG2 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 an AF488-conjugated secondary antibody (green) in PBS at room temperature in the dark. Phalloidin - AF594 was used to stain Actin filaments (red). DAPI was used to stain the cell nuclei (blue).
Product Name:Recombinant Anti-BCL2 Rabbit mAb
Cat No:CMA1199
Source:Rabbit
Reactivity:H, M, R
Applications:WB, IH, IF/IC
*Application Key:
H - Human, M - Mouse, R - Rat, B - Bovine, C - Chicken, D - Dog, G - Goat, Mk - Monkey, P - Pig, Rb - Rabbit, S - Sheep, Z - Zebrafish
*Species Reactivity Key:
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
Size
Price(USD)
200 μl
350
100 μl
220
30 μl
110
50 μl
150
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Description:Recombinant rabbit monoclonal antibody to BCL2
Immunogen:KLH-conjugated synthetic peptide encompassing a sequence within the center region of human BCL2. The exact sequence is proprietary.
Purification:This antibody is purified through a protein G column.
Clonality:Monoclonal
Form:Liquid in PBS, pH 7.3, 50% glycerol, and 0.05% Proclin300.
Dilution:WB (1/1000 - 1/3000), IH (1/100 - 1/300), IF/IC (1/100 - 1/300)
Gene Symbol:BCL2
Alternative Names:Apoptosis regulator Bcl-2
Entrez Gene (Human): 596;
Entrez Gene (Mouse): 12043;
Entrez Gene (Rat): 24224;
SwissProt (Human): P10415;
SwissProt (Mouse): P10417;
SwissProt (Rat): P49950;
Storage/Stability:Shipped at 4°C. Upon delivery aliquot and store at -20°C for one year. Avoid freeze/thaw cycles.
  • Western blot analysis of BCL2 expression in H1792 (A), A2780 (B), HUT78 (C), mouse spleen (D), mouse kidney (E), rat spleen (F), rat kidney (G) whole cell lysates. (Predicted band size: 26 kD; Observed band size: 26 kD)
  • Immunohistochemical analysis of BCL2 staining in human stomach 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. Tyramide-AF488 (green) was used as the chromogen. The section was then counterstained with DAPI (blue).
  • Immunofluorescent analysis of BCL2 staining in HepG2 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 an AF488-conjugated secondary antibody (green) in PBS at room temperature in the dark. Phalloidin - AF594 was used to stain Actin filaments (red). DAPI was used to stain the cell nuclei (blue).
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