Date published: 2026-4-1

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Cdk7 Antibody (MO-1): sc-56284

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Datasheets
  • Cdk7 Antibody (MO-1) is a mouse monoclonal IgG2b κ, cited in 8 publications, provided at 200 µg/ml
  • raised against the C-terminus of Cdk7 of human origin
  • recommended for detection of Cdk7 of mouse, rat and human origin by WB, IP, IF and FCM
  • available conjugated to either phycoerythrin or FITC for IF, IHC(P) and FCM
  • See Cdk7 (C-4): sc-7344 for Cdk7 antibody conjugates, including AC, HRP, FITC, PE, Alexa Fluor® 488, 594, 647, 680 and 790.
  • m-IgG Fc BP-HRP is the preferred secondary detection reagent for Cdk7 Antibody (MO-1) for WB applications. This reagent is now offered in a bundle with Cdk7 Antibody (MO-1) (see ordering information below).
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Cdk7 Antibody (MO-1) is a mouse monoclonal IgG2b antibody that detects Cdk7 in mouse, rat, and human samples through applications such as western blotting (WB), immunoprecipitation (IP), immunofluorescence (IF), and flow cytometry (FCM). Cdk7 plays a pivotal role in the regulation of the cell cycle by functioning as a cyclin-dependent kinase-activating kinase (CAK), which is essential for the activation of other cyclin-dependent kinases, including Cdk2 and Cdc2. This activation is crucial for the progression of cells through the cell cycle, as it ensures that the necessary phosphorylation events occur at specific threonine residues, such as Thr 160 in Cdk2 and Thr 161 in Cdc2. Cdk7 is located in the nucleus, where Cdk7 interacts with various cyclins, including cyclin H, which is vital for its activation. Proper functioning of Cdk7 is important not only for cell cycle regulation but also for transcriptional regulation, as Cdk7 phosphorylates the carboxy-terminal domain of RNA polymerase II, thereby facilitating the transcription process. Anti-Cdk7 antibody (MO-1) is an invaluable tool for researchers studying cell cycle dynamics and the intricate signaling pathways that govern cellular proliferation and differentiation.

For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Cdk7 Antibody (MO-1)

sc-56284
200 µg/ml
$322.00

Cdk7 Antibody (MO-1): m-IgG Fc BP-HRP Bundle

sc-551938
200 µg Ab; 10 µg BP
$361.00

Cdk7 Antibody (MO-1) FITC

sc-56284 FITC
200 µg/ml
$336.00

Cdk7 Antibody (MO-1) PE

sc-56284 PE
200 µg/ml
$349.00

How can Cdk7 (MO-1): sc-56284 mouse monoclonal antibody be used for double or triple staining, if the other primary antibodies are also raised in mouse?

Asked by: Germaine
In this case, we recommend using a directly conjugated mouse monoclonal primary antibody. This antibody is available conjugated to phycoerythrin (sc-56284 PE) or fluoroscein (sc-56284 FITC).
Answered by: Technical Support
Date published: 2017-02-27
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Rated 5 out of 5 by from Goof for WB and IPIt is good for Western blot and IP with human cell nuclear extract.
Date published: 2018-02-04
Rated 5 out of 5 by from Good resultWe use it for IF applications and got good result.
Date published: 2016-12-02
Rated 5 out of 5 by from Good specificityGood specificity, it is suitable for my current experimental study, unexpected results
Date published: 2016-11-23
Rated 5 out of 5 by from Good specificityGood specificity and signal strength for WB in NIH/3T3 and K-562 whole cell lysates. -SCBT QGood specificity and signal strength for WB in NIH/3T3 and K-562 whole cell lysates. -SCBT QCC
Date published: 2016-11-05
Rated 4 out of 5 by from Works well for IF applicationsWorks well for IF applications, positive in HeLa. -SCBT QC
Date published: 2015-04-01
Rated 5 out of 5 by from WB positive with SW480 cellsWB positive with SW480 cells. -SCBT Publication Review
Date published: 2015-02-26
Rated 4 out of 5 by from Worked with transfected lysate by WBWorked with transfected lysate by WB -SCBT QC
Date published: 2015-02-05
Rated 4 out of 5 by from Good specificity and signal strength forGood specificity and signal strength for WB in NIH/3T3 and K-562 whole cell lysates. -SCBT QC
Date published: 2014-07-16
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Cdk7 Antibody (MO-1) is rated 4.6 out of 5 by 8.
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