Anti-CDK1 + CDK2 + CDK3 + CDK5 (phospho Y15) antibody [EPR7875] - BSA and Azide free (ab248508)
Key features and details
- Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
- Rabbit monoclonal [EPR7875] to CDK1 + CDK2 + CDK3 + CDK5 (phospho Y15) - BSA and Azide free
- Suitable for: ELISA, IHC-P, WB, Dot blot
- Reacts with: Mouse, Rat, Human, Recombinant fragment
Overview
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Product name
Anti-CDK1 + CDK2 + CDK3 + CDK5 (phospho Y15) antibody [EPR7875] - BSA and Azide free -
Description
Rabbit monoclonal [EPR7875] to CDK1 + CDK2 + CDK3 + CDK5 (phospho Y15) - BSA and Azide free -
Host species
Rabbit -
Specificity
The antibody will cross-react with phosphorylated CDK1 (pY15), CDK2 (pY15), CDK3 (pY15) and CDK5 (pY15) but not with non-phosphorylated CDK1, CDK2, CDK3 and CDK5. Please see our ELISA results on the images section.
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Tested applications
Suitable for: ELISA, IHC-P, WB, Dot blotmore details -
Species reactivity
Reacts with: Mouse, Rat, Human, Recombinant fragment -
Immunogen
Synthetic peptide. This information is proprietary to Abcam and/or its suppliers.
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General notes
ab248508 is the carrier-free version of ab133463.
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
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 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 production
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
Properties
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Form
Liquid -
Storage instructions
Shipped at 4°C. Store at +4°C. Do Not Freeze. -
Dissociation constant (KD)
KD = 4.10 x 10 -11 M Learn more about KD -
Storage buffer
pH: 7.2
Constituent: PBS -
Carrier free
Yes -
Concentration information loading...
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Purity
Protein A purified -
Clonality
Monoclonal -
Clone number
EPR7875 -
Isotype
IgG -
Research areas
Images
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Anti-CDK1 + CDK2 + CDK3 + CDK5 (phospho Y15) antibody [EPR7875] (ab133463) at 1/1000 dilution (purified) + HeLa cell lysate treated with UV at 10 µg
Secondary
HRP goat anti-rabbit (H+L) at 1/1000 dilution
Predicted band size: 34 kDa
Observed band size: 34 kDaThis data was developed using ab133463, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer: 5% NFDM/TBST.
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This data was developed using ab133463, the same antibody clone in a different buffer formulation.
Immunohistochemical staining of paraffin embedded human colon with purified ab133463 at a working dilution of 1 in 75. The secondary antibody used is a HRP polymer for rabbit IgG. The sample is counter-stained with hematoxylin. Antigen retrieval was perfomed using Tris-EDTA buffer, pH 9.0. PBS was used instead of the primary antibody as the negative control, and is shown in the inset. -
This data was developed using ab133463, the same antibody clone in a different buffer formulation.
Direct ELISA antibody dose-response curve using purified ab133463 at 0-1000 ng/ml. Antigen concentration of 1000 ng/mL. An alkaline phosphatase-conjugated goat anti-rabbit IgG (H+L) (1/2500) was used as the secondary antibody. -
This data was developed using ab133463, the same antibody clone in a different buffer formulation.
Direct ELISA antibody dose-response curve using purified ab133463 at 0-1000 ng/ml. Antigen concentration of 1000 ng/mL. An alkaline phosphatase-conjugated goat anti-rabbit IgG (H+L) (1/2500) was used as the secondary antibody. -
Anti-CDK1 + CDK2 + CDK3 + CDK5 (phospho Y15) antibody [EPR7875] (ab133463) at 1/2000 dilution (purified) + C6 cell lysate at 10 µg
Secondary
HRP goat anti-rabbit (H+L) at 1/1000 dilution
Predicted band size: 34 kDa
Observed band size: 34 kDaThis data was developed using ab133463, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer: 5% NFDM/TBST.
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Anti-CDK1 + CDK2 + CDK3 + CDK5 (phospho Y15) antibody [EPR7875] (ab133463) at 1/2000 dilution (purified) + NIH/3T3 cell lysate at 10 µg
Secondary
HRP goat anti-rabbit (H+L) at 1/1000 dilution
Predicted band size: 34 kDa
Observed band size: 34 kDaThis data was developed using ab133463, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer: 5% NFDM/TBST.
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This data was developed using ab133463, the same antibody clone in a different buffer formulation.
Dot blot analysis of CDK1+CDK2+CDK3+CDK5 (pY15) phospho peptide (lane 1) and CDK1+CDK2+CDK3+CDK5 non-phospho peptide (lane 2) labelling CDK1+CDK2+CDK3+CDK5 (phospho Y15) with unpurified ab133463 at a dilution of 1/1000. A peroxidase-conjugated goat anti-rabbit IgG (H+L) was used as the secondary antibody (1/2500). Blocking and dilution buffer: 5% NFDM/TBST. Exposure time: 10 seconds. -
This data was developed using ab133463, the same antibody clone in a different buffer formulation.
Saso2 cells were incubated at 37°C for 24 hours with vehicle control (0 µM) and different concentrations of Amifostine (ab141060). Decreased expression of CDK1 (phospho Y15) (unpurified ab133463) in Saso2 cells correlates with an increase in Amifostine concentration, as described in literature.
Whole cell lysates were prepared with RIPA buffer (containing protease inhibitors and sodium orthovanadate), 10µg of each were loaded on the gel and the WB was run under reducing conditions. After transfer the membrane was blocked for an hour using 5% BSA before being incubated with unpurified ab133463 at 1 µg/ml and ab32384 at 1 µg/ml overnight at 4°C. Antibody binding was detected using an anti-rabbit antibody conjugated to HRP (ab97051) at 1/10000 and visualised using ECL development solution.
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This data was developed using ab133463, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin embedded human breast carcinoma tissue labelling CDK1+CDK2+CDK3+CDK5 with unpurified ab133463 at 1/50 dilution. Heat mediated antigen retrieval was performed with citrate buffer pH 6 before commencing with IHC staining protocol. -
Anti-CDK1 + CDK2 + CDK3 + CDK5 (phospho Y15) antibody [EPR7875] (ab133463) at 1/1500 dilution (unpurified) + NIH/3T3 cell lysate at 1/1000 dilution
Secondary
HRP goat anti-rabbit (H+L) at 1/1000 dilution
Predicted band size: 34 kDa
Observed band size: 34 kDaThis data was developed using ab133463, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer: 5% NFDM/TBST.
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Anti-CDK1 + CDK2 + CDK3 + CDK5 (phospho Y15) antibody [EPR7875] (ab133463) at 1/1500 dilution (unpurified) + C6 cell lysate at 10 µg
Secondary
HRP goat anti-rabbit (H+L) at 1/1000 dilution
Predicted band size: 34 kDa
Observed band size: 34 kDaThis data was developed using ab133463, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer: 5% NFDM/TBST.
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This data was developed using ab133463, the same antibody clone in a different buffer formulation.Equilibrium disassociation constant (KD)
Learn more about KD
Click here to learn more about KD
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All lanes : Anti-CDK1 + CDK2 + CDK3 + CDK5 (phospho Y15) antibody [EPR7875] (ab133463) at 1/1000 dilution (unpurified)
Lane 1 : HeLa cell lysate
Lane 2 : HeLa cell lysate treated with UV
Lysates/proteins at 10 µg per lane.
Secondary
All lanes : HRP labelled goat anti-rabbit IgG at 1/2000 dilution
Predicted band size: 34 kDa
Observed band size: 34 kDaThis data was developed using ab133463, the same antibody clone in a different buffer formulation.
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This data was developed using ab133463, the same antibody clone in a different buffer formulation.Immunohistochemical staining of paraffin embedded human colon with unpurified ab133463 at a working dilution of 1 in 50. The secondary antibody used is a HRP polymer for rabbit IgG. The sample is counter-stained with hematoxylin. Antigen retrieval was perfomed using Tris-EDTA buffer, pH 9.0. PBS was used instead of the primary antibody as the negative control, and is shown in the inset.
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