Anti-BACH2 antibody [EPR28026-43]
- BOND RX™ Validated
- 20ul selling size
- Recombinant
- RabMAb
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(1 Publication)
Rabbit Recombinant Monoclonal BACH2 antibody. Suitable for I-ELISA, Flow Cyt (Intra), WB, IHC-P and reacts with Recombinant fragment - Human, Human, Mouse samples. Cited in 1 publication.
View Alternative Names
Transcription regulator protein BACH2, BTB and CNC homolog 2, BACH2
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-BACH2 antibody [EPR28026-43] (AB320721)
Immunohistochemical analysis of paraffin-embedded Human Non-Hodgkin's lymphoma tissue labeling BACH2 with ab320721 at 1/100 (5.08 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on human Non-Hodgkin's lymphoma. The section was incubated with ab320721 for 30 mins at room temperature.
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-BACH2 antibody [EPR28026-43] (AB320721)
Immunohistochemical analysis of paraffin-embedded Human pancreas tissue labeling BACH2 with ab320721 at 1/100 (5.08 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control : no staining on human pancreas. The section was incubated with ab320721 for 30 mins at room temperature.
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
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-BACH2 antibody [EPR28026-43] (AB320721)
Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized Human PBMC (human peripheral blood mononuclear cell) cells labelling BACH2 with ab320721 at 1/500 dilution (0.1ug) / Right compared with a Rabbit monoclonal IgG (ab172730) / Left isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody).
Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/5000 dilution was used as the secondary antibody.
Gated on viable CD14+ Monocytes.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-BACH2 antibody [EPR28026-43] (AB320721)
Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized NAMALWA (human Burkitt's lymphoma B lymphocyte) (Right) / HL-60 (human acute promyelocytic leukemia promyeloblast) (Left) cells labelling BACH2 with ab320721 at 1/50 dilution (1ug) (Red) compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody).
Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/5000 dilution was used as the secondary antibody.
Negative control : HL-60 (PMID : 10949928).
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-BACH2 antibody [EPR28026-43] (AB320721)
Immunohistochemical analysis of paraffin-embedded Human tonsil tissue labeling BACH2 with ab320721 at 1/100 (5.08 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on B cells of human tonsil (PMID : 14982850; PMID : 24277074). The section was incubated with ab320721 for 30 mins at room temperature.
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
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-BACH2 antibody [EPR28026-43] (AB320721)
Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized Ramos (human Burkitt's lymphoma B lymphocyte) (Right) / THP-1 (human monocytic leukemia monocyte) (Left) cells labelling BACH2 with ab320721 at 1/50 dilution (1ug) (Red) compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody).
Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/5000 dilution was used as the secondary antibody.
Negative control : THP-1 (PMID : 10949928).
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-BACH2 antibody [EPR28026-43] (AB320721)
Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized Human PBMC (human peripheral blood mononuclear cell) cells labelling BACH2 with ab320721 at 1/500 dilution (0.1ug) / Right compared with a Rabbit monoclonal IgG (ab172730) / Left isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody).
Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/5000 dilution was used as the secondary antibody.
Gated on viable CD19+ Lymphocytes.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-BACH2 antibody [EPR28026-43] (AB320721)
Immunohistochemical analysis of paraffin-embedded (A) Ramos (human Burkitt's lymphoma B lymphocyte) cell pellet. (B) THP-1 (human monocytic leukemia monocyte) cell pellet. tissue labeling BACH2 with ab320721 at 1/2000 (0.254 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on (A) Ramos (human Burkitt's lymphoma B lymphocyte) cell pellet, negative staining on (B) THP-1 (human monocytic leukemia monocyte) cell pellet. The section was incubated with ab320721 for 30 mins at room temperature.
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
- I-ELISA
Supplier Data
Indirect ELISA - Anti-BACH2 antibody [EPR28026-43] (AB320721)
Indirect ELISA analysis of ab320721 at 1000-0 ng/ml. The Secondary antibody used was Alkaline Phosphatase-conjugated AffiniPure Goat Anti-Rabbit IgG (H+L) at 1 : 2500 dilution.
Antigen : Human BACH2,Human BACH1.
Antigen concentration : 1000 ng/ml
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-BACH2 antibody [EPR28026-43] (AB320721)
Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized Mouse PBMC cells labelling BACH2 with ab320721 at 1/500 dilution (0.1ug) / Right compared with a Rabbit monoclonal IgG (ab172730) / Left isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody).
Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/5000 dilution was used as the secondary antibody.
Gated on viable CD19+ Lymphocytes
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-BACH2 antibody [EPR28026-43] (AB320721)
Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized Mouse PBMC cells labelling BACH2 with ab320721 at 1/500 dilution (0.1ug) / Right compared with a Rabbit monoclonal IgG (ab172730) / Left isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody). Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/5000 dilution was used as the secondary antibody. Gated on viable CD14+ Monocytes.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-BACH2 antibody [EPR28026-43] (AB320721)
Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized WEHI-231 (mouse B cell lymphoma B lymphocyte) (Right) / J774A.1 (mouse reticulum cell sarcoma monocyte/macrophage) (Left) cells labelling BACH2 with ab320721 at 1/50 dilution (1ug) (Red) compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody).
Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/5000 dilution was used as the secondary antibody.
Low expression : J774A.1.
- WB
Supplier Data
Western blot - Anti-BACH2 antibody [EPR28026-43] (AB320721)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Negative control : THP-1, HL-60 (PMID : 10949928).
To minimize protein degradation, cells were lysed immediately after harvest and then applied to a gel and transfer membrane for Western blotting as soon as possible in lanes 5-6.
The bands (in lanes 1-2) beneath the target band are likely to be degraded target fragments.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
Exposure time : Lanes 1-4 : 15 seconds, Lanes 5-6 : 26 seconds
All lanes:
Western blot - Anti-BACH2 antibody [EPR28026-43] (ab320721) at 1/1000 dilution
Lane 1:
Ramos (human Burkitts lymphoma B lymphocyte) whole cell lysate at 20 µg
Lanes 2 and 5:
NAMALWA (human Burkitts lymphoma B lymphocyte) whole cell lysate at 20 µg
Lanes 3 and 6:
THP-1 (human monocytic leukemia monocyte) whole cell lysate at 20 µg
Lane 4:
HL-60 (human acute promyelocytic leukemia promyeloblast) whole cell lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Observed band size: 60 kDa,120 kDa,36 kDa
false
- WB
Supplier Data
Western blot - Anti-BACH2 antibody [EPR28026-43] (AB320721)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Low expression : J774A.1.
The bands beneath the target band are likely to be degraded target fragments.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
All lanes:
Western blot - Anti-BACH2 antibody [EPR28026-43] (ab320721) at 1/1000 dilution
Lane 1:
WEHI-231 (mouse B cell lymphoma B lymphocyte ) whole cell lysate at 20 µg
Lane 2:
J774A.1 (mouse reticulum cell sarcoma monocyte/macrophage) whole cell lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Observed band size: 60 kDa,120 kDa,36 kDa
false
Exposure time: 81s
Reactivity data
Product details
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
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.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
BACH2 plays an important role in the regulation of immune responses. It functions as a homodimer or forms heterodimers with other proteins such as BACH1 allowing it to modulate gene expression effectively. BACH2 regulates the balance between immune tolerance and activation by controlling the production of cytokines and the differentiation of T cells. This regulation is important for preventing autoimmune responses while enabling proper immune responses against infections.
Pathways
BACH2 participates actively in the oxidative stress response and pathways of lymphocyte development. In the oxidative stress pathway it interacts with proteins like KEAP1 and NRF2 to regulate antioxidant gene expression. In lymphocyte development it influences the recombination of immunoglobulin genes and supports the maturation of B cells into plasma cells. By doing so BACH2 ensures the proper functioning of the immune system working in conjunction with various transcriptional regulatory networks.
Product protocols
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Target data
Publications (1)
Recent publications for all applications. Explore the full list and refine your search
The Journal of biological chemistry 300:107842 PubMed39357823
2024
Applications
Unspecified application
Species
Unspecified reactive species
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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