Anti-Cdk1 + Cdk2 (phospho T14) antibody [EPR17499] - BSA and Azide free
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal CDK1 phospho T14 antibody. Carrier free. Suitable for IP, Dot, WB, IHC-P and reacts with Human, Mouse, Rat, Synthetic peptide samples.
View Alternative Names
CDC2, CDC28A, CDKN1, P34CDC2, CDK1, Cyclin-dependent kinase 1, Cell division control protein 2 homolog, Cell division protein kinase 1, p34 protein kinase
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Cdk1 + Cdk2 (phospho T14) antibody [EPR17499] - BSA and Azide free (AB250674)
This data was developed using ab183550, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded rat spleen tissue labeling Cdk1 + Cdk2 (phospho T14) with ab183550 at 1/250 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) secondary antibody at 1/500 dilution. Nuclear and cytoplasmic staining on lymphocytes of rat spleen tissue is observed. Counter stained with Hematoxylin.
Negative control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Cdk1 + Cdk2 (phospho T14) antibody [EPR17499] - BSA and Azide free (AB250674)
This data was developed using ab183550, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human colonic adenocarcinoma tissue labeling Cdk1 + Cdk2 (phospho T14) with ab183550 at 1/250 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) secondary antibody at 1/500 dilution. Nuclear and cytoplasmic staining on cancer cells of Human colonic adenocarcinoma tissue is observed. Counter stained with Hematoxylin.
Negative control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Cdk1 + Cdk2 (phospho T14) antibody [EPR17499] - BSA and Azide free (AB250674)
This data was developed using ab183550, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded mouse spleen tissue labeling Cdk1 + Cdk2 (phospho T14) with ab183550 at 1/250 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) secondary antibody at 1/500 dilution. Nuclear and cytoplasmic staining on lymphocytes of mouse spleen tissue is observed. Counter stained with Hematoxylin.
Negative control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Cdk1 + Cdk2 (phospho T14) antibody [EPR17499] - BSA and Azide free (AB250674)
This data was developed using ab183550, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human colon tissue labeling Cdk1 + Cdk2 (phospho T14) with ab183550 at 1/250 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) secondary antibody at 1/500 dilution. Scattered nuclear and cytoplasmic staining on epithelial cells of Human colon tissue is observed. Counter stained with Hematoxylin.
Negative control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- IP
Supplier Data
Immunoprecipitation - Anti-Cdk1 + Cdk2 (phospho T14) antibody [EPR17499] - BSA and Azide free (AB250674)
This data was developed using ab183550, the same antibody clone in a different buffer formulation.
Cdk1 + Cdk2 (phospho T14) was immunoprecipitated from 1mg of HeLa (Human epithelial cells from cervix adenocarcinoma) whole cell extract with ab183550 at 1/40 dilution. Western blot was performed from the immunoprecipitate using ab183550 at 1/1000 dilution. Anti-Rabbit IgG (HRP), specific to the non-reduced form of IgG, was used as secondary antibody at 1/1000 dilution.
Lane 1 (Input) : HeLa whole cell extract 10 μg (Input).
Lane 2 : ab183550 IP in HeLa whole cell extract.
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab183550 in HeLa whole cell extract.
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
All lanes:
Immunoprecipitation - Anti-Cdk1 + Cdk2 (phospho T14) antibody [EPR17499] (<a href='/en-us/products/primary-antibodies/cdk1-cdk2-phospho-t14-antibody-epr17499-ab183550'>ab183550</a>)
false
- Dot
Supplier Data
Dot Blot - Anti-Cdk1 + Cdk2 (phospho T14) antibody [EPR17499] - BSA and Azide free (AB250674)
This data was developed using ab183550, the same antibody clone in a different buffer formulation.
Dot blot analysis of Cdk1 + Cdk2 (phospho T14) peptide (Lane 1), and non-phospho peptide (Lane 2), labeled using ab183550 at 1/1000 dilution, followed by Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated secondary antibody at 1/1000 dilution.
Blocking/Dilution buffer : 5% NFDM/TBST.
Exposure time = 3 minutes
Related conjugates and formulations (1)
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Anti-Cdk1 + Cdk2 (phospho T14) antibody [EPR17499]
Reactivity data
Product details
ab250674 is the carrier-free version of ab183550.
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.
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
Cdks are pivotal in driving cell cycle phases collaborating with cyclins to regulate checkpoints at G1/S and G2/M transitions. Cdk1 primarily associates with cyclin B to facilitate the entry into mitosis whereas Cdk2 partners with cyclin E and cyclin A to advance the G1/S transition. Their activity is indispensable for proper cell cycle regulation and any misregulation can lead to uncontrolled cell proliferation. Importantly their involvement in complex formation ensures orderly progression and coordination across cell cycle stages.
Pathways
Cdk1 and Cdk2 integrate into the cell cycle regulation pathways and the DNA damage response pathways. In the cell cycle pathway Cdks are required for the orderly progression and checkpoints that ensure proper mitotic entry and DNA synthesis. Similarly in response to DNA damage these kinases work closely with proteins like p21 which can inhibit Cdk activity to halt cell cycle progression and facilitate DNA repair. By coordinating with related proteins like cyclins and p21 Cdk1 and Cdk2 help maintain genomic integrity through effective cell cycle control.
Product protocols
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Target data
Additional targets
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