Anti-53BP1 antibody [HL275]
- Recombinant
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Rabbit Recombinant Monoclonal 53BP1 antibody. Carrier free. Suitable for IHC-P, ICC/IF, WB and reacts with Human, Mouse, Rat, Cat, Dog samples. Immunogen corresponding to Synthetic Peptide within Human TP53BP1.
View Alternative Names
TP53-binding protein 1, 53BP1, p53-binding protein 1, p53BP1, TP53BP1
- IHC-P
Supplier Data
Immunohistochemistry paraffin embedded sections - Anti-53BP1 antibody [HL275] (AB308375)
Immunohistochemical analysis of human breast carcinoma tissue labeling 53BP1 using ab308375 at 1/200 dilution. Antigen retrival was performed using Citrate buffer, pH 6.0, 15 min
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-53BP1 antibody [HL275] (AB308375)
For immunofluorescence analysis, HeLa cells were fixed in 4% paraformaldehyde at room temperature for 15 minutes and permeabilized for detection of 53BP1 protein using ab308375 at 1/1000 dilution (green). Nuclei (blue) is stained with fluoroshield with DAPI.
- IHC-P
Supplier Data
Immunohistochemistry paraffin embedded sections - Anti-53BP1 antibody [HL275] (AB308375)
Immunohistochemical analysis of mouse urinary bladder, cerebellum, thymus gland and mouse brain tissue labeling 53BP1 using ab308375 at 1/100 dilution. Antigen retrival was performed using Citrate buffer, pH 6.0, 15 min
- IHC-P
Supplier Data
Immunohistochemistry paraffin embedded sections - Anti-53BP1 antibody [HL275] (AB308375)
Immunohistochemical analysis of rat thymus gland and brain tissue labeling 53BP1 using ab308375 at 1/100 dilution. Antigen retrival was performed using Citrate buffer, pH 6.0, 15 min
- WB
Supplier Data
Western blot - Anti-53BP1 antibody [HL275] (AB308375)
HeLa whole cell and nuclear extracts (30 μg) were separated by 5% SDS-PAGE, and the membrane was blotted with 53BP1 antibody [HL36] (ab308375) diluted at 1/1000. A HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.
All lanes:
Western blot - Anti-53BP1 antibody [HL275] (ab308375) at 1/1000 dilution
Lane 1:
HeLa cell lysate at 30 µg
Lane 2:
HeLa nuclear extract at 30 µg
Secondary
All lanes:
HRP-conjugated anti-rabbit IgG antibody
Predicted band size: 213.6 kDa
false
- WB
Supplier Data
Western blot - Anti-53BP1 antibody [HL275] (AB308375)
Various whole cell extracts (30 μg) were separated by 5% SDS-PAGE, and the membrane was blotted with 53BP1 antibody [HL36] (ab308375) diluted at 1/1000. A HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.
All lanes:
Western blot - Anti-53BP1 antibody [HL275] (ab308375) at 1/1000 dilution
Lane 1:
HEK293T cell lysate at 30 µg
Lane 2:
A431 cell lysate at 30 µg
Lane 3:
HeLa cell lysate at 30 µg
Lane 4:
HepG2 cell lysate at 30 µg
Secondary
All lanes:
HRP-conjugated anti-rabbit IgG antibody
Predicted band size: 213.6 kDa
false
- WB
Supplier Data
Western blot - Anti-53BP1 antibody [HL275] (AB308375)
Various whole cell extracts (30 μg) were separated by 5% SDS-PAGE, and the membrane was blotted with 53BP1 antibody [HL36] (ab308375) diluted at 1/1000. A HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.
All lanes:
Western blot - Anti-53BP1 antibody [HL275] (ab308375) at 1/1000 dilution
Lane 1:
Neuro2A cell lysate at 30 EU/µg/L
Lane 2:
NIH-3T3 cell lysate at 30 µg
Lane 3:
Raw264.7 cell lysate at 30 µg
Lane 4:
C2C12 cell lysate at 30 µg
Secondary
All lanes:
HRP-conjugated anti-rabbit IgG antibody
Predicted band size: 213.6 kDa
false
- WB
Supplier Data
Western blot - Anti-53BP1 antibody [HL275] (AB308375)
Various whole cell extracts (30 μg) were separated by 5% SDS-PAGE, and the membrane was blotted with 53BP1 antibody [HL36] (ab308375) diluted at 1/1000. A HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.
All lanes:
Western blot - Anti-53BP1 antibody [HL275] (ab308375) at 1/1000 dilution
Lane 1:
PC12 cell lysate at 30 µg
Lane 2:
Rat2 cell lysate at 30 µg
Secondary
All lanes:
HRP-conjugated anti-rabbit IgG antibody
Predicted band size: 213.6 kDa
false
- WB
Supplier Data
Western blot - Anti-53BP1 antibody [HL275] (AB308375)
Various whole cell extracts (30 μg) were separated by 5% SDS-PAGE, and the membrane was blotted with 53BP1 antibody [HL36] (ab308375) diluted at 1/1000. A HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.
All lanes:
Western blot - Anti-53BP1 antibody [HL275] (ab308375) at 1/1000 dilution
Lane 1:
MDCK cell lysate at 30 µg
Lane 2:
PG4 cell lysate at 30 µg
Secondary
All lanes:
HRP-conjugated anti-rabbit IgG antibody
Predicted band size: 213.6 kDa
false
Reactivity data
Product details
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.
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
As a DNA damage response mediator 53BP1 functions to recognize and bind to sites of double-strand breaks in DNA promoting non-homologous end joining (NHEJ). This protein is a component of a larger protein complex that recruits factors necessary for DNA repair. Its interaction with DNA lesions also involves chromatin remodeling aiming to facilitate successful repair of the DNA. 53BP1 works in concert with other proteins such as H2AX and MDC1.
Pathways
Researchers observe 53BP1 in processes such as the DNA damage checkpoint and repair pathways. This protein significantly contributes to the pathways involved in maintaining cell cycle checkpoints. It interacts with proteins like ATM and BRCA1 coordinating the cellular response to DNA damage and ensuring that genomic integrity checks occur properly before cell cycle progression continues. These interactions place 53BP1 at a pivotal position in decision-making between repair pathways.
Product protocols
- Visit the General protocols
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Target data
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com