Rabbit Recombinant Monoclonal p150 CAF1/CAF antibody. Carrier free. Suitable for WB, Flow Cyt (Intra), ICC/IF, IHC-P and reacts with Human samples.
IgG
Rabbit
pH: 7.2 - 7.4
Constituents: 100% PBS
Liquid
Monoclonal
WB | Flow Cyt (Intra) | ICC/IF | IHC-P | |
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Human | Tested | Tested | Tested | Tested |
Species | Dilution info | Notes |
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Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes Perform heat-mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol. |
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Core component of the CAF-1 complex, a complex that is thought to mediate chromatin assembly in DNA replication and DNA repair. Assembles histone octamers onto replicating DNA in vitro. CAF-1 performs the first step of the nucleosome assembly process, bringing newly synthesized histones H3 and H4 to replicating DNA; histones H2A/H2B can bind to this chromatin precursor subsequent to DNA replication to complete the histone octamer. It may play a role in heterochromatin maintenance in proliferating cells by bringing newly synthesized cbx proteins to heterochromatic DNA replication foci.
Chromatin assembly factor 1 subunit A, CAF-1 subunit A, Chromatin assembly factor I p150 subunit, CAF-I 150 kDa subunit, CAF-I p150, hp150, CAF1P150, CAF, CHAF1A
Rabbit Recombinant Monoclonal p150 CAF1/CAF antibody. Carrier free. Suitable for WB, Flow Cyt (Intra), ICC/IF, IHC-P and reacts with Human samples.
IgG
Rabbit
pH: 7.2 - 7.4
Constituents: 100% PBS
Liquid
Monoclonal
Yes
EPR5576(2)
Affinity purification Protein A
Blue Ice
+4°C
Do Not Freeze
ab232030 is the carrier-free version of Anti-p150 CAF1/CAF antibody [EPR5576(2)] ab126625.
Mouse, Rat: We have preliminary internal testing data to indicate this antibody may not react with these species. Please contact us for more information.
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
This product is a recombinant monoclonal antibody, which offers several advantages including:
For more information, read more on recombinant antibodies.
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. The carrier-free buffer and high concentration allow for increased conjugation efficiency.
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.
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.
This supplementary information is collated from multiple sources and compiled automatically.
The p150 CAF1 also known as CAF protein and CAF1 protein is part of the chromatin assembly factor 1 complex. It weighs approximately 150 kDa. This protein primarily expresses in the nucleus of eukaryotic cells where it plays an important role in DNA replication and repair. The p150 protein acts as a structural component that is essential for proper chromatin assembly during the S phase of the cell cycle.
This target functions as part of the CAF-1 complex which includes two additional subunits—p60 and p48. The complex aids in the assembly of newly synthesized histones onto replicating DNA facilitating nucleosome formation. It affects chromatin dynamics influencing transcriptional regulation by providing nucleosome assembly binding sites along DNA. This process maintains genomic integrity during cell division and influences gene expression in response to various cell signals.
The p150 protein interacts within pathways involved in DNA replication and repair. It plays a major role in the nucleosome assembly pathway closely interacting with histone proteins H3 and H4. Through these interactions it ensures the stability of replication forks during DNA synthesis. Besides it participates in the regulation of the cell cycle and influences the chromatin assembly pathway important for accurate DNA replication and cell division.
Several conditions show connection with the p150 protein's function in DNA replication. Alterations or defects in its expression link to cancer where chromatin misassembly leads to genomic instability a hallmark of tumorigenesis. Additionally the involvement of p150 in neurodegenerative disorders sheds light on how disrupted chromatin assembly can affect neural cells. Its interaction with proteins like retinoblastoma (Rb) points to the potential dysregulation in cell cycle control further influencing disease progression.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
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In the unlikely event of one of our products not working as expected, you are covered by our product promise.
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All lanes: Western blot - Anti-p150 CAF1/CAF antibody [EPR5576(2)] (Anti-p150 CAF1/CAF antibody [EPR5576(2)] ab126625) at 1/10000 dilution
Lane 1: HeLa (Human cervix adenocarcinoma epithelial cell) whole cell lysate
Lane 2: HeLa (Human cervix adenocarcinoma epithelial cell) starved 24 hours and treated with 500ng/ml nocodazole for 24 hours whole cell lysate
Lane 3: MCF7 (Human breast adenocarcinoma epithelial cell) whole cell lysate
Lane 4: K-562 (Human chronic myelogenous leukemia lymphoblast) whole cell lysate
All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/20000 dilution
Predicted band size: 107 kDa
This data was developed using ab232030, the same antibody clone in a different buffer formulation.
Flow Cytometry analysis of HeLa (Human cervix adenocarcinoma epithelial cell) cells labelling p150 CAF1/CAF with Purified ab232030 at 1:20 dilution (10 μg/ml) (Red). Cells were fixed with 4% Paraformaldehyde and permeabilised with 90% Methanol. A Goat anti rabbit IgG (Alexa Fluor® 488, Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) secondary antibody was used at 1:2000. Isotype control - Rabbit monoclonal IgG (Black). Unlabelled control - Cell without incubation with primary antibody and secondary antibody (Blue).
This data was developed using Anti-p150 CAF1/CAF antibody [EPR5576(2)] ab126625, the same antibody clone in a different buffer formulation.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of human colon tissue sections labeling p150 CAF1/CAF with Purified Anti-p150 CAF1/CAF antibody [EPR5576(2)] ab126625 at 1:150 (0.9 μg/ml). Heat mediated antigen retrieval was performed using Heat mediated antigen retrieval using Bond™ Epitope Retrieval Solution 2 (pH 9.0) . Tissue was counterstained with Hematoxylin. Rabbit specific IHC polymer detection kit HRP/DAB (Rabbit specific IHC polymer detection kit HRP/DAB ab209101) secondary antibody was used at 1:0 dilution. PBS instead of the primary antibody was used as the negative control.
This data was developed using ab232030, the same antibody clone in a different buffer formulation.
Immunocytochemistry analysis of HT-29 (Human colorectal adenocarcinoma epithelial cell) cells labeling p150 CAF1/CAF with Purified ab232030 at 1:50 dilution (2.7 μg/ml). Cells were fixed in 4% Paraformaldehyde and permeabilized with 0.1% tritonX-100. Cells were counterstained with Alexa Fluor® 594 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker ab195889 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594) 1:200 (2.5 μg/ml). Goat anti rabbit IgG (Alexa Fluor® 488, Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) was used as the secondary antibody at 1:1000 (2 μg/ml) dilution. DAPI (blue) was used as nuclear counterstain. PBS instead of the primary antibody was used as the secondary antibody only control.
This data was developed using Anti-p150 CAF1/CAF antibody [EPR5576(2)] ab126625, the same antibody clone in a different buffer formulation.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of human breast carcinoma tissue sections labeling p150 CAF1/CAF with Purified Anti-p150 CAF1/CAF antibody [EPR5576(2)] ab126625 at 1:150 (0.9 μg/ml). Heat mediated antigen retrieval was performed using Heat mediated antigen retrieval using Bond™ Epitope Retrieval Solution 2 (pH 9.0) . Tissue was counterstained with Hematoxylin. Rabbit specific IHC polymer detection kit HRP/DAB (Rabbit specific IHC polymer detection kit HRP/DAB ab209101) secondary antibody was used at 1:0 dilution. PBS instead of the primary antibody was used as the negative control.
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