Anti-Bim antibody [Y36] - Mouse IgG2a (Chimeric) - BSA and Azide free
- Recombinant
- KO Validated
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Mouse Recombinant Monoclonal Bim antibody. Carrier free. Suitable for WB, ICC/IF, IHC-P and reacts with Human, Mouse, Rat samples.
View Alternative Names
BIM, BCL2L11, Bcl-2-like protein 11, Bcl2-L-11, Bcl2-interacting mediator of cell death
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-Bim antibody [Y36] - Mouse IgG2a (Chimeric) - BSA and Azide free (AB324661)
This data was developed using ab324516, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized Raji (human Burkitt's lymphoma B lymphocyte) cells labelling Bim with ab324516 at 1/100 (9.4 ug/ml) dilution, followed by ab150117 Goat Anti-Mouse IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 (2 ug/ml) dilution (Green).
Confocal image showing cytoplasmic staining in Raji and no staining in WI-38 cell line (shown in green). The counterstain was observed in magenta. Nuclear DNA was labelled with DAPI (shown in blue).
Negative control : WI-38.
Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
ab202272 Recombinant Alexa Fluor® 594 Anti-alpha Tubulin antibody [EP1332Y] - Microtubule Marker (ab202272) was used to counterstain tubulin at 1/200 (2.5 ug/ml) dilution (Magenta).
Secondary antibody only control : Secondary antibody is ab150117 Goat Anti-Mouse IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 ug/ml) dilution.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-Bim antibody [Y36] - Mouse IgG2a (Chimeric) - BSA and Azide free (AB324661)
This data was developed using ab324516, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized A20 (mouse reticulum sarcoma B lymphocyte) cells labelling Bim with ab324516 at 1/100 (9.4 ug/ml) dilution, followed by ab150117 Goat Anti-Mouse IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 (2 ug/ml) dilution (Green).
Confocal image showing cytoplasmic staining in A20 and no staining in B16-F10 cell line (shown in green). The counterstain was observed in magenta. Nuclear DNA was labelled with DAPI (shown in blue).
Negative control : B16-F10.
Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
ab202272 Recombinant Alexa Fluor® 594 Anti-alpha Tubulin antibody [EP1332Y] - Microtubule Marker (ab202272) was used to counterstain tubulin at 1/200 (2.5 ug/ml) dilution (Magenta).
Secondary antibody only control : Secondary antibody is ab150117 Goat Anti-Mouse IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 ug/ml) dilution.
- WB
Supplier Data
Western blot - Anti-Bim antibody [Y36] - Mouse IgG2a (Chimeric) - BSA and Azide free (AB324661)
This data was developed using ab324516, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Low expression : WI-38 and B16-F10
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
All lanes:
Western blot - Anti-Bim antibody [Y36] - Mouse IgG2a (Chimeric) (ab324516) at 1/1000 dilution
Lane 1:
Raji (human Burkitt's lymphoma B lymphocyte) at 20 µg
Lane 2:
WI-38 (human fetal lung fibroblast) at 20 µg
Lane 3:
HEK-293 (human embryonic kidney epithelial cell) at 20 µg
Lane 4:
HeLa (human cervical adenocarcinoma epithelial cell) at 20 µg
Lane 5:
A20 (mouse reticulum sarcoma B lymphocyte) at 20 µg
Lanes 6 - 7:
4T1 (mouse mammary gland carcinoma epithelial cell) at 20 µg
Secondary
All lanes:
Peroxidase-Conjugated Goat anti-Mouse IgG (H+L) at 1/10000 dilution
false
Exposure time: 180s
- WB
Supplier Data
Western blot - Anti-Bim antibody [Y36] - Mouse IgG2a (Chimeric) - BSA and Azide free (AB324661)
This data was developed using ab324516, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
The molecular weight observed is consistent with what has been described in the literature (PMID : 24872388).
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
Exposure time : Lanes 1-4 : 125 seconds; Lane 5 : 37 seconds; Lanes 6-7 : 180 seconds
All lanes:
Western blot - Anti-Bim antibody [Y36] - Mouse IgG2a (Chimeric) (ab324516) at 1/1000 dilution
Lane 1:
Human spleen tissue lysates at 20 µg
Lane 2:
Human thyroid tissue lysates at 20 µg
Lane 3:
Rat spleen tissue lysates at 20 µg
Lane 4:
Rat testis tissue lysates at 20 µg
Lane 5:
Mouse spleen tissue lysates at 20 µg
Lane 6:
Wild-type HAP1 (human chronic myelogenous leukemia near-haploid cell) whole cell lysate at 20 µg
Lane 7:
BCL2L11 knockout HAP1 whole cell lysate at 20 µg
Secondary
All lanes:
Peroxidase-Conjugated Goat anti-Mouse IgG (H+L) at 1/5000 dilution
false
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Bim antibody [Y36] - Mouse IgG2a (Chimeric) - BSA and Azide free (AB324661)
This data was developed using ab324516, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human breast cancer tissue labeling Bim with ab324516 at 1/500 (1.874 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on human breast cancer. The primary antibody was incubated for 30 mins at room temperature, followed by anti-mouse IgG2a antibody for 8 mins at room temperature during the LeicaDS9800 kit staining procedure.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Bim antibody [Y36] - Mouse IgG2a (Chimeric) - BSA and Azide free (AB324661)
This data was developed using ab324516, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Panel A Wild-type HAP1 (Human chronic myelogenous leukemia near-haploid cell) cell pellet and Panel B BCL2L11 knockout HAP1 cell pellet labeling Bim with ab324516 at 1/500 (1.874 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on (Panel A) wild-type HAP1 cell pellet, no staining on (Panel B) BCL2L11 knockout HAP1 cell pellet. The primary antibody was incubated for 30 mins at room temperature, followed by anti-mouse IgG2a antibody for 8 mins at room temperature during the LeicaDS9800 kit staining procedure.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Bim antibody [Y36] - Mouse IgG2a (Chimeric) - BSA and Azide free (AB324661)
This data was developed using ab324516, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human lung cancer tissue labeling Bim with ab324516 at 1/500 (1.874 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on human lung cancer. The primary antibody was incubated for 30 mins at room temperature, followed by anti-mouse IgG2a antibody for 8 mins at room temperature during the LeicaDS9800 kit staining procedure.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
Related conjugates and formulations (1)
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Anti-Bim antibody [Y36] - Mouse IgG2a (Chimeric)
Reactivity data
Product details
ab324661 is the carrier-free version of ab324516.
This mouse monoclonal chimeric antibody has been engineered from a RabMAb parent antibody (ab32158). By necessity, some rabbit sequence is retained as part of the variable domain. When multiplexing with other rabbit-derived antibodies, using cross absorbed Fc-reactive secondary antibodies are recommended.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
Properties and storage information
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Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Storage information
Product protocols
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Target data
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Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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