Anti-Bim 抗体 [Y36]

• IHC-P

Unknown

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Bim antibody [Y36] (AB32158)

ab32158 staining Bim in human breast cancer tissue sections by Immunohistochemistry (IHC-P - paraformaldehyde-fixed, paraffin-embedded sections). Antigen retrieval was by heat mediated antigen retrieval using Tris/EDTA Buffer, PH9 (ab93684). Samples were incubated with primary antibody (1/100 in blocking buffer) and a Biotin-conjugated Donkey anti-rabbit IgG polyclonal (1/500) was used as the secondary antibody. Cytoplasmic staining can be seen in the human breast cancer cells. Hematoxylin was used as a counter stain.

• Flow Cyt (Intra)

Unknown

Flow Cytometry (Intracellular) - Anti-Bim antibody [Y36] (AB32158)

Intracellular Flow Cytometry analysis of A431 (human epidermoid carcinoma) cells labelling Bim with ab32158 at 1/50 (red). Cells were fixed with 4% paraformaldehyde and permeabilised with 90% methanol. An Alexa Fluorr^®488-conjugated goat anti-rabbit IgG (1/2000) was used as the secondary antibody. Black - Isotype control, rabbit monoclonal IgG. Blue - Unlabelled control, cells without incubation with primary and secondary antibodies.

• Flow Cyt (Intra)

Unknown

Flow Cytometry (Intracellular) - Anti-Bim antibody [Y36] (AB32158)

Overlay histogram showing HAP1 wildtype (green line) and HAP1-BCL2L11 knockout cells (red line) stained with ab32158. The cells were fixed 80% methanol (5 min), and then permeabilized with 0.1% PBS-Triton X-100 for 15 min. The cells were then incubated in 1x PBS / 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (ab32158, 1μg/ml) for 30 min at 22°C. The secondary antibody used was Alexa Fluor^® 488 goat anti-rabbit IgG (H&L) presorbed (ab150081) at 1/2000 dilution for 30 min at 22°C. A rabbit IgG1 isotype control antibody (ab172730) was used at the same concentration and conditions as the primary antibody (HAP1 wildtype - black line, HAP1-BCL2L11 knockout - grey line). Unlabelled sample was also used as a control (this line is not shown for the purpose of simplicity). Acquisition of >5,000 events were collected using a 50 mW Blue laser (488nm) and 530/30 bandpass filter.

• ICC/IF

Unknown

Immunocytochemistry/ Immunofluorescence - Anti-Bim antibody [Y36] (AB32158)

Immunocytochemistry/Immunofluorescence analysis of A20 (Mouse reticulum sarcoma cell line) labeling Bim with ab32158 at a dilution of 1/250. Cells were fixed with 100% methanol. ab150077 (1/1000) was used as the secondary antibody. Cells were co-stained with ab7291, a mouse anti-tubulin antibody (1/200) using ab150120 as the secondary. Nuclei were counterstained with DAPI (blue).

Secondary antibody only control, cells without incubation with the primary antibody was used as negative control.

Confocal image showing cytoplasmic staining on A20 cell line

• WB

Lab

Western blot - Anti-Bim antibody [Y36] (AB32158)

Lane 1 : Wild type HAP1 whole cell lysate (20 μg)
Lane 2 : Bim knockout HAP1 whole cell lysate (20 μg)
Lane 3 : Raji whole cell lysate (20 μg)
Lane 4 : Jurkat whole cell lysate (20 μg)

Lanes 1 - 4 : Merged signal (red and green). Green - ab32158 observed at 25 kDa. Red - loading control, ab9484, observed at 37 kDa.

ab32158 was shown to specifically react with Bim when Bim knockout samples were used. Wild-type and Bim knockout samples were subjected to SDS-PAGE. ab32158 and ab9484 (Mouse anti-GAPDH loading control) were incubated overnight at 4°C at 1/500 dilution and 1/10000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye^® 800CW) preabsorbed ab216773 and Goat anti-Mouse IgG H&L (IRDye^® 680RD) preabsorbed ab216776 secondary antibodies at 1/10000 dilution for 1 hour at room temperature before imaging.

All lanes:

Western blot - Anti-Bim antibody [Y36] (ab32158)

Predicted band size: 22 kDa

false

• WB

Lab

Western blot - Anti-Bim antibody [Y36] (AB32158)

Observed band size : 22, 18 kDa

Exposure time : Lane 1- 5 : 3 minutes; Lane 6 : 2 seconds

Blocking/Diluting buffer and concentration : 5% NFDM /TBST

The observed molecular weight is consistent with the literature (PMID : 24872388)

All lanes:

Western blot - Anti-Bim antibody [Y36] (ab32158) at 1/2000 dilution

Lane 1:

Raji (human Burkitt's lymphoma) whole cell lysate at 20 µg

Lane 2:

A431 (human epidermoid carcinoma) whole cell lysate at 20 µg

Lane 3:

Molt-4 (human acute lymphoblastic leukemia) whole cell lysate at 20 µg

Lane 4:

Human thymus tissue lysate at 20 µg

Lane 5:

Mouse thymus tissue lysate at 20 µg

Lane 6:

A20 (mouse reticulum cell sarcoma) whole cell lysate at 20 µg

Secondary

All lanes:

Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution

Predicted band size: 22 kDa

false

• WB

AbReview16685****

Western blot - Anti-Bim antibody [Y36] (AB32158)

Primary diluted in PBS (5% BSA + 0.1% tween20) and incubated with sample for 1 hour and 30 minutes at 20°C.

All lanes:

Western blot - Anti-Bim antibody [Y36] (ab32158) at 1/500 dilution

All lanes:

Whole cell lysates prepared from human jurkat cells at 200000 Cells

Secondary

All lanes:

HRP conjugated Donkey polyclonal to rabbit IgG at 1/2000 dilution

Predicted band size: 22 kDa

Observed band size: 22 kDa

true

Exposure time: 30s

This image is courtesy of an anonymous abreview.

• WB

Lab

Western blot - Anti-Bim antibody [Y36] (AB32158)

Observed band size : 22, 18 kDa

Exposure time : Lane 1-3 : 3 minutes; Lane 4 : 10 seconds

Blocking/Diluting buffer and concentration : 5% NFDM /TBST

The observed molecular weight is consistent with the literature (PMID : 24872388)

All lanes:

Western blot - Anti-Bim antibody [Y36] (ab32158) at 1/2000 dilution

Lane 1:

Mouse spleen tissue lysate at 10 µg

Lane 2:

Rat spleen tissue lysate at 10 µg

Lane 3:

PC-12 (rat adrenal gland pheochromocytoma) whole cell lysate at 10 µg

Lane 4:

Raw264.7 (mouse abelson murine leukemia virus-induced tumor) whole cell lysate at 10 µg

Secondary

All lanes:

Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution

Predicted band size: 22 kDa

false

• ICC/IF

Unknown

Immunocytochemistry/ Immunofluorescence - Anti-Bim antibody [Y36] (AB32158)

Immunocytochemistry/Immunofluorescence analysis of Raji (Human Burkitt's lymphoma cell line) labeling Bim with ab32158 at a dilution of 1/250. Cells were fixed with 100% methanol. ab150077 (1/1000) was used as the secondary antibody. Cells were co-stained with ab7291, a mouse anti-tubulin antibody (1/200) using ab150120 as the secondary. Nuclei were counterstained with DAPI (blue).

Secondary antibody only control, cells without incubation with the primary antibody was used as negative control.

Confocal image showing cytoplasmic staining on Raji cell line

• Flow Cyt (Intra)

Unknown

Flow Cytometry (Intracellular) - Anti-Bim antibody [Y36] (AB32158)

Intracellular Flow Cytometry analysis of Raji (human Burkitt's lymphoma) whole cell lysate labeling Bim with ab32158 at 1/100 (red). Cells were fixed with 4% paraformaldehyde. An Alexa Fluorr^® 488)-conjugated goat anti-rabbit IgG (1/2000) was used as the secondary antibody. Black - Isotype control, rabbit monoclonal IgG (ab172730). Blue - Unlabelled control, cells without incubation with primary and secondary antibodies.

• IP

Unknown

Immunoprecipitation - Anti-Bim antibody [Y36] (AB32158)

ab32158 at 1/50 immunoprecipitating Bim in Raji (human Burkitt's lymphoma) whole cell lysate.

Lane 1 (input) : Raji whole cell lysate (10μg)

Lane 2 (+) : ab32158 + Raji whole cell lysate.

Lane 3 (-) : Rabbit monoclonal IgG (ab172730) instead of ab32158 in Raji whole cell lysate.

For western blotting, ab32158 (1/1000) was used as the primary antibody and ab131366 VeriBlot for IP Detection Reagent (HRP) was used for detection (1/10 000).

Blocking buffer and concentration : 5% NFDM/TBST.

Diluting buffer and concentration : 5% NFDM /TBST.

All lanes:

Immunoprecipitation - Anti-Bim antibody [Y36] (ab32158)

Predicted band size: 22 kDa

Observed band size: 22 kDa

false

Exposure time: 3min