Bim Recombinant Rabbit Monoclonal Antibody [SU0318] - BSA and Azide free
Catalog# HA750137
Bim Recombinant Rabbit Monoclonal Antibody [SU0318] - BSA and Azide free
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WB
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IF-Cell
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IHC-P
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IP
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FC
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Human
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Mouse
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unconjugated
Overview
Product Name
Bim Recombinant Rabbit Monoclonal Antibody [SU0318] - BSA and Azide free
Antibody Type
Recombinant Rabbit monoclonal Antibody
Immunogen
Synthetic peptide within human Bim aa 1-40.
Species Reactivity
Human, Mouse
Validated Applications
WB, IF-Cell, IHC-P, IP, FC
Target Molecular Weight
Predicted band size: 22 kDa
Positive Control
Raji cell lysate, HeLa cell lysate, MCF7 cell lysate, RAW264.7 cell lysate, Hela, A431, HepG2, human kidney tissue, RAW264.7, MCF7.
Conjugation
unconjugated
Clone Number
SU0318
Product Features
Form
Liquid
Concentration
1mg/ml
Storage Instructions
Store at 2-8℃. Avoid freeze.
Storage Buffer
1*PBS (pH7.4).
Isotype
IgG
Purification Method
Protein A affinity purified.
Application Dilution
Target
Function
Bcl-2-like protein 11, commonly called BIM, is a protein that in humans is encoded by the BCL2L11 gene. The protein encoded by this gene belongs to the BCL-2 protein family. BCL-2 family members form hetero- or homodimers and act as anti- or pro-apoptotic regulators that are involved in a wide variety of cellular activities. The protein encoded by this gene contains a Bcl-2 homology domain 3 (BH3). It has been shown to interact with other members of the BCL-2 protein family, including BCL2, BCL2L1/BCL-X(L), and MCL1, and to act as an apoptotic activator. The expression of this gene can be induced by nerve growth factor (NGF), as well as by the forkhead transcription factor FKHR-L1 (FoxO3a), which suggests a role of this gene in neuronal and lymphocyte apoptosis. Transgenic studies of the mouse counterpart suggested that this gene functions as an essential initiator of apoptosis in thymocyte-negative selection. Several alternatively spliced transcript variants of this gene have been identified.
Background References
1. Liu L et al. SIRT2 enhances 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced nigrostriatal damage via apoptotic pathway. Front Aging Neurosci 6:184 (2014).
2. Ontikatze T et al. Dihydroartemisinin is a Hypoxia-Active Anti-Cancer Drug in Colorectal Carcinoma Cells. Front Oncol 4:116 (2014).
Sequence Similarity
Belongs to the Bcl-2 family.
Tissue Specificity
Isoform BimEL, isoform BimL and isoform BimS are the predominant isoforms and are widely expressed with tissue-specific variation. Isoform Bim-gamma is most abundantly expressed in small intestine and colon, and in lower levels in spleen, prostate, testis, heart, liver and kidney.
Post-translational Modification
Phosphorylation at Ser-69 by MAPK1/MAPK3 leads to interaction with TRIM2 and polyubiquitination, followed by proteasomal degradation. Deubiquitination catalyzed by USP27X stabilizes the protein (By similarity).; Ubiquitination by TRIM2 following phosphorylation by MAPK1/MAPK3 leads to proteasomal degradation. Conversely, deubiquitination catalyzed by USP27X stabilizes the protein.
Subcellular Location
Endomembrane system, Mitochondrion.
Synonyms
BCL2 like 11 antibody
B2L11_HUMAN antibody
BAM antibody
Bcl 2 interacting protein Bim antibody
Bcl 2 related ovarian death agonist antibody
Bcl-2-like protein 11 antibody
BCL2 interacting mediator of cell death antibody
BCL2 like 11 (apoptosis facilitator) antibody
BCL2 like protein 11 antibody
Bcl2-interacting mediator of cell death antibody
ExpandImages
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This data was developed using ET1608-14, the same antibody clone in a different buffer formulation.
Western blot analysis of Bim on different lysates with Rabbit anti-Bim antibody (ET1608-14) at 1/5,000 dilution.
Lane 1: Raji cell lysate
Lane 2: HeLa cell lysate
Lane 3: MCF7 cell lysate
Lane 4: RAW264.7 cell lysate
Lysates/proteins at 15 µg/Lane.
Predicted band size: 22 kDa
Observed band size: 25 kDa
Exposure time: 3 minutes 49 seconds;
4-20% SDS-PAGE gel.
Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (ET1608-14) at 1/5,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature. -
This data was developed using ET1608-14, the same antibody clone in a different buffer formulation.
ICC staining of Bim in Hela cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 1% Blocker BSA for 15 minutes at room temperature. Cells were probed with the primary antibody (ET1608-14, 1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue). -
This data was developed using ET1608-14, the same antibody clone in a different buffer formulation.
ICC staining of Bim in A431 cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 1% Blocker BSA for 15 minutes at room temperature. Cells were probed with the primary antibody (ET1608-14, 1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue). -
This data was developed using ET1608-14, the same antibody clone in a different buffer formulation.
ICC staining of Bim in HepG2 cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 1% Blocker BSA for 15 minutes at room temperature. Cells were probed with the primary antibody (ET1608-14, 1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue). -
This data was developed using ET1608-14, the same antibody clone in a different buffer formulation.
Application: Immunohistochemistry (IHC-P)
Species: Human
Tissue: Kidney
Sample: Paraffin-embedded section
Antigen retrieval: Heat-mediated, Tris-EDTA buffer (pH 9.0), 20 minutes at 95℃.
Wash buffer: 1× TBST
Endogenous peroxidase blocking: 3% H₂O₂, 10 minutes at room temperature.
Blocking: 1% BSA + 10% normal goat serum, 10 minutes at room temperature.
Primary antibody: ET1608-14, 1/200, 1 hour at room temperature.
Secondary antibody: HA1119, 20 minutes at room temperature. -
This data was developed using ET1608-14, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of RAW264.7 cells labeling Bim.
Cells were fixed and permeabilized. Then stained with the primary antibody (ET1608-14, 1μg/mL) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody (HA1121) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black). -
This data was developed using ET1608-14, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of MCF7 cells labeling Bim.
Cells were fixed and permeabilized. Then stained with the primary antibody (ET1608-14, 1μg/mL) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody (HA1121) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"
Products with the same target and pathway
Bim Rabbit Polyclonal Antibody
Application: WB,IP,IF,IHC-P
Reactivity: Human,Mouse,Rat
Conjugate: unconjugated
