Anti-p60 CAF1/MPP7 antibody [EPR6105] - BSA and Azide free
- RabMAb
- Recombinant
- What is this?
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(1 Publication)
Rabbit Recombinant Monoclonal p60 CAF1/MPP7 antibody. Carrier free. Suitable for IHC-P, IP, WB, Flow Cyt (Intra) and reacts with Human samples. Cited in 1 publication.
View Alternative Names
CAF1A, CAF1P60, MPHOSPH7, MPP7, CHAF1B, Chromatin assembly factor 1 subunit B, CAF-1 subunit B, Chromatin assembly factor I p60 subunit, M-phase phosphoprotein 7, CAF-I 60 kDa subunit, CAF-I p60
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-p60 CAF1/MPP7 antibody [EPR6105] - BSA and Azide free (AB226065)
This data was developed using ab109442, the same antibody clone in a different buffer formulation.
ab109442 at 1/250 dilution staining p60 CAF1/MPP7 in paraffin-embedded Human colon tissue.
Perform heat mediated antigen retrieval via the pressure cooker method before commencing with IHC staining protocol.
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-p60 CAF1/MPP7 antibody [EPR6105] - BSA and Azide free (AB226065)
This data was developed using ab109442, the same antibody clone in a different buffer formulation.
ab109442 at 1/250 dilution staining p60 CAF1/MPP7 in paraffin-embedded Human tonsil tissue.
Perform heat mediated antigen retrieval via the pressure cooker method before commencing with IHC staining protocol.
- Flow Cyt (Intra)
Lab
Flow Cytometry (Intracellular) - Anti-p60 CAF1/MPP7 antibody [EPR6105] - BSA and Azide free (AB226065)
This data was developed using ab109442, the same antibody clone in a different buffer formulation.Overlay histogram showing HeLa cells stained with ab109442 (red line). The cells were fixed with 80% methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab109442, 1/1000 dilution) for 30 min at 22°C. The secondary antibody used was Alexa Fluor® 488 goat anti-rabbit IgG (H&L) (ab150077) at 1/2000 dilution for 30 min at 22°C. Isotype control antibody (black line) was rabbit IgG (monoclonal) (0.1µg/1x106 cells) used under the same conditions. Unlabelled sample (blue line) was also used as a control. Acquisition of >5,000 events were collected using a 20mW Argon ion laser (488nm) and 525/30 bandpass filter.
- IP
Lab
Immunoprecipitation - Anti-p60 CAF1/MPP7 antibody [EPR6105] - BSA and Azide free (AB226065)
This data was developed using ab109442, the same antibody clone in a different buffer formulation. p60 CAF1/MPP7 was immunoprecipitated from 0.35 mg HeLa (Human cervix adenocarcinoma epithelial cell) whole cell lysate 10 μg with 109442 at 1/50 dilution (2μg). VeriBlot for IP Detection Reagent (HRP) (ab131366) was used at 1/5000 dilution.
Lane 1 : HeLa (Human cervix adenocarcinoma epithelial cell) whole cell lysate 10 μg
Lane 2 : ab109442 IP in HeLa whole cell lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab109442 in HeLa whole cell lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
All lanes:
Immunoprecipitation - Anti-p60 CAF1/MPP7 antibody [EPR6105] (<a href='/en-us/products/primary-antibodies/p60-caf1-mpp7-antibody-epr6105-ab109442'>ab109442</a>)
Predicted band size: 61 kDa
Observed band size: 70 kDa
false
- WB
Unknown
Western blot - Anti-p60 CAF1/MPP7 antibody [EPR6105] - BSA and Azide free (AB226065)
This data was developed using ab109442, the same antibody clone in a different buffer formulation.
All lanes:
Western blot - Anti-p60 CAF1/MPP7 antibody [EPR6105] (<a href='/en-us/products/primary-antibodies/p60-caf1-mpp7-antibody-epr6105-ab109442'>ab109442</a>)
Lane 1:
Jurkat cell lysate at 10 µg
Lane 2:
HeLa cell lysate at 10 µg
Lane 3:
293T cell lysate at 10 µg
Lane 4:
Caco-2 cell lysate at 10 µg
Predicted band size: 61 kDa
Observed band size: 70 kDa
false
Related conjugates and formulations (1)
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Anti-p60 CAF1/MPP7 antibody [EPR6105]
Reactivity data
Product details
ab226065 is the carrier-free version of ab109442.
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.
Species reactivity
Rat: We have preliminary internal testing data to indicate this antibody may not react with this species.
Please contact us for more information.
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
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
In cellular environments MPP7 is significant in maintaining cell polarity and epithelial cell junctions. It plays an important part in forming the Crumbs-3 (CRB3) complex an essential component regulating epithelial cell polarity. Through this complex MPP7 collaborates closely with PATJ (Pals1-associated tight junction protein) and DLG1 (Discs Large Homolog 1) contributing to cell junction stability and signal transduction pathways that regulate epithelial integrity.
Pathways
MPP7 is integral to epithelial cell polarity pathways and cell adhesion signaling. It affects pathway activities by coordinating with proteins like DLG1 and PATJ. By aligning with the CRB3 complex MPP7 influences processes within the Hippo signaling pathway a pathway that controls cell proliferation and apoptosis. This positions MPP7 as a mediator balancing cell growth and communication in complex signaling networks.
Product protocols
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Target data
Publications (1)
Recent publications for all applications. Explore the full list and refine your search
Scientific reports 15:18296 PubMed40419589
2025
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'.
For licensing inquiries, please contact partnerships@abcam.com