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ab18624 |
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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
Detects a band at 26 kDa in Jurkat cell lysate that represents Bcl2.
IHC-P, ICC/IF, WBmore details
Reacts with
Mouse, Human
Predicted to work with
Rat, Dog
Synthetic peptide conjugated to KLH derived from within residues 1 - 100 of Human Bcl2.
(Peptide available as ab18624.)
Liquid
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
Preservative: 0.02% Sodium Azide
Constituents: 1% BSA, PBS, pH 7.4
Concentration information loading...
Immunogen affinity purified
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 ab18210 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
IHC-P: Use at an assay dependent concentration. (PubMed: 21624358)
ICC/IF: Use a concentration of 1 µg/ml
WB: Use a concentration of 1 µg/mlDetects a band of approximately 26 kDa.Can be blocked with Bcl2 peptide (ab18624).
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).
Western blot - Bcl2 antibody (ab18210)

All lanes : Anti-Bcl2 antibody (ab18210) at 1 µg/ml
Lane 1 : Jurkat cell lysate
Lane 2 : Jurkat cell lysate with Bcl2 peptide (ab18624) at 1 µg/ml
Lysates/proteins at 20 µg per lane.
Secondary
Alexa Fluor Goat polyclonal to Rabbit IgG (700) at 1/5000 dilution
Performed under reducing conditions.
Observed band size : 26 kDa (why is the actual band size different from the predicted?)
Additional bands at : 60 kDa (possible cross reactivity).
ab18210 recognizes a band of 26 kDa corresponding to Bcl2. A non-specific band of ~ 60 kDa is also detected. Both bands are quenched by the addition of the immunizing peptide (ab18624).
Immunocytochemistry/ Immunofluorescence - Bcl2 antibody (ab18210)

ICC/IF image of ab18210 stained human HeLa cells. The cells were methanol fixed (5 min) and incubated with the antibody (ab18210, 1µg/ml) for 1h at room temperature. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Image-iTTM FX Signal Enhancer was used as the primary blocking agent, 5% BSA (in TBS-T) was used for all other blocking steps. DAPI was used to stain the cell nuclei (blue).
This product has been referenced in:
See all 5 publications for this product
Publishing research using ab18210? Please let us know so that we can cite the reference in this datasheet
Concentration of lot no. is
Concentration not available for this lot.
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All lanes : Anti-Bcl2 antibody (ab18210) at 1 µg/ml
Lane 1 : Jurkat cell lysate
Lane 2 : Jurkat cell lysate with Bcl2 peptide (ab18624) at 1 µg/ml
Lysates/proteins at 20 µg per lane.
Secondary
Alexa Fluor Goat polyclonal to Rabbit IgG (700) at 1/5000 dilution
Performed under reducing conditions.
Observed band size : 26 kDa (why is the actual band size different from the predicted?)
Additional bands at : 60 kDa (possible cross reactivity).
ab18210 recognizes a band of 26 kDa corresponding to Bcl2. A non-specific band of ~ 60 kDa is also detected. Both bands are quenched by the addition of the immunizing peptide (ab18624).

ICC/IF image of ab18210 stained human HeLa cells. The cells were methanol fixed (5 min) and incubated with the antibody (ab18210, 1µg/ml) for 1h at room temperature. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Image-iTTM FX Signal Enhancer was used as the primary blocking agent, 5% BSA (in TBS-T) was used for all other blocking steps. DAPI was used to stain the cell nuclei (blue).

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