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Read our guarantee »Products:Cell Biology >> Apoptosis >> Intracellular >> Bcl2 Family
Anti-Bcl2 antibody
See all Bcl2 products (30) ...
Rabbit polyclonal to Bcl2
Reacts with Bcl-2
IHC-P, IHC-Fr, ICC, IP, WBmore details
Reacts with
Mouse, Rat, Cow, Human
Synthetic peptide: AGRTGYDNREIVMKYIHY, corresponding to N terminal amino acids 1-18 of Human Bcl2.
AGRTGYDNRE IVMKYIHY
WB: HeLa, HL-60 and Jurkat lysate IHC: mouse cerebral cortex, cerebellum, hippocampus
Liquid
Store at +4°C. Do not freeze.
PBS with 0.1% sodium azide
Concentration information loading...
IgG fraction
Polyclonal
IgG
Cancer >> Cancer Metabolism >> Cellular metabolic process
Cancer >> Cancer Metabolism >> Response to hypoxia
Cancer >> Tumor biomarkers >> Oncoproteins
Cancer >> Oncoproteins/suppressors >> Oncoproteins >> Cell survival & death
Cancer >> Invasion/microenvironment >> Apoptosis >> Bcl 2 family
Signal Transduction >> Metabolism >> Mitochondrial
Cell Biology >> Apoptosis >> Intracellular >> Bcl2 Family
Our Abpromise guarantee covers the use of ab7973 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
IHC-P: 1/100Perform heat mediated antigen retrieval via the microwave method before commencing with IHC staining protocol.(PubMed: 20800980In successful cases, the following protocol was used. Before the beginning of the procedure, slides should be put in a 200 ml Coplin jar filled with 10 mM citrate buffer and heated in a commercial microwave oven operating at a frequency of 2.45 GHz and 600 W power setting. After two heating cycles of 5 minutes each, slides should be allowed to cool at room temperature and thoroughly washed in phosphate buffered saline (PBS) pH 7.4 0.1 M.)
IHC-Fr: 1/100(We have data to suggest that this antibody works on paraffin sections, however, we would recommed to use frozen sections and cannot guarantee IHC-P.)
ICC: Use at an assay dependent dilution.
IP: Use at an assay dependent dilution.
WB: 1/100
Suppresses apoptosis in a variety of cell systems including factor-dependent lymphohematopoietic and neural cells. Regulates cell death by controlling the mitochondrial membrane permeability. Appears to function in a feedback loop system with caspases. Inhibits caspase activity either by preventing the release of cytochrome c from the mitochondria and/or by binding to the apoptosis-activating factor (APAF-1).
Expressed in a variety of tissues.
Note=A chromosomal aberration involving BCL2 has been found in chronic lymphatic leukemia. Translocation t(14;18)(q32;q21) with immunoglobulin gene regions. BCL2 mutations found in non-Hodgkin lymphomas carrying the chromosomal translocation could be attributed to the Ig somatic hypermutation mechanism resulting in nucleotide transitions.
Belongs to the Bcl-2 family.
The BH4 motif is required for anti-apoptotic activity and for interaction with RAF-1.
Phosphorylation/dephosphorylation on Ser-70 regulates anti-apoptotic activity. Growth factor-stimulated phosphorylation on Ser-70 by PKC is required for the anti-apoptosis activity and occurs during the G2/M phase of the cell cycle. In the absence of growth factors, BCL2 appears to be phosphorylated by other protein kinases such as ERKs and stress-activated kinases. Dephosphorylated by protein phosphatase 2A (PP2A).
Proteolytically cleaved by caspases during apoptosis. The cleaved protein, lacking the BH4 motif, has pro-apoptotic activity, causes the release of cytochrome c into the cytosol promoting further caspase activity.
Monoubiquitinated by PARK2, leading to increase its stability.
Mitochondrion outer membrane. Nucleus membrane. Endoplasmic reticulum membrane.
Target information above from: UniProt accessionP10415
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Immunohistochemistry (Paraffin-embedded sections) - Bcl2 antibody (ab7973)

Fixation: 4% paraformaldehyde, paraffin embedding. Before the beginning of the procedure, slides are put in a 200 ml Coplin jar filled with 10 mM citrate buffer and heated in a commercial microwave oven operating at a frequency of 2.45 GHz and 600 W power setting. After two heating cycles of 5 minutes each, slides are allowed to cool at room temperature and thoroughly washed in phosphate buffered saline (PBS) pH 7.4 0.1 M. ABC peroxidase + Nickel intensification. Conterstaining Methyl green
Prof. Adalberto Merighi, Veterinary School, Univ. of Torino, Italy
Immunohistochemistry (Paraffin-embedded sections) - Bcl2 antibody (ab7973)

Sample treated using same protocol described in the above image.
Prof. Adalberto Merighi, Veterinary School, Univ. of Torino, Italy
Immunohistochemistry (Paraffin-embedded sections) - Bcl2 antibody (ab7973)

Sample treated using same protocol described in the above image, except with no countertaining.
Prof. Adalberto Merighi, Veterinary School, Univ. of Torino, Italy
Western blot - Bcl2 antibody (ab7973)

Anti-Bcl2 antibody (ab7973) at 1/500 dilution + 25 ug HeLa whole cell lysate
Secondary
Goat anti rabbit HRP at 1/4000 dilution
This image is an edited version of an image submitted courtesy of an anonymous Abreview on 30 September 2005. We do not have any further information relating to this image.
Immunocytochemistry/ Immunofluorescence-Bcl2 antibody(ab7973)

ICC/IF image of ab7973 stained MCF7 cells. The cells were 4% PFA fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab7973, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
This product has been referenced in:
See all 11 publications for this product
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Fixation: 4% paraformaldehyde, paraffin embedding. Before the beginning of the procedure, slides are put in a 200 ml Coplin jar filled with 10 mM citrate buffer and heated in a commercial microwave oven operating at a frequency of 2.45 GHz and 600 W power setting. After two heating cycles of 5 minutes each, slides are allowed to cool at room temperature and thoroughly washed in phosphate buffered saline (PBS) pH 7.4 0.1 M. ABC peroxidase + Nickel intensification. Conterstaining Methyl green
Prof. Adalberto Merighi, Veterinary School, Univ. of Torino, Italy

Sample treated using same protocol described in the above image.
Prof. Adalberto Merighi, Veterinary School, Univ. of Torino, Italy

Sample treated using same protocol described in the above image, except with no countertaining.
Prof. Adalberto Merighi, Veterinary School, Univ. of Torino, Italy

Anti-Bcl2 antibody (ab7973) at 1/500 dilution + 25 ug HeLa whole cell lysate
Secondary
Goat anti rabbit HRP at 1/4000 dilution
This image is an edited version of an image submitted courtesy of an anonymous Abreview on 30 September 2005. We do not have any further information relating to this image.

ICC/IF image of ab7973 stained MCF7 cells. The cells were 4% PFA fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab7973, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.

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