Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
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Species reactivity: | Human |
Applications: | IF-Cell, FC |
Clonality: | Monoclonal |
Clone number: | JJ203-01 |
Form: | Liquid |
Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. Avoid repeated freeze / thaw cycles. |
Storage buffer: | 1*TBS (pH7.4), 0.05% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide. |
Concentration: | 1ug/ul |
Purification: | Protein A affinity purified. |
Molecular weight: | Predicted band size: 39 kDa |
Isotype: | IgG |
Immunogen: | Recombinant protein within Human Cdk7 aa 151-346 / 346. |
Positive control: | HeLa, A431, HepG2, 293. |
Subcellular location: | Nucleus, Cytoplasm, perinuclear region. |
Recommended Dilutions:
IF-Cell FC |
1:100-1:500 1:50-1:100 |
Uniprot #: | SwissProt: P50613 Human |
Alternative names: | 39 kDa protein kinase CAK CAK1 Cdk activating kinase CDK-activating kinase 1 CDK-activating kinase cdk7 CDK7_HUMAN CDKN7 Cell division protein kinase 7 Cyclin dependent kinase 7 cyclin-dependent kinase 7 (MO15 homolog, Xenopus laevis, cdk-activating kinase) Cyclin-dependent kinase 7 HCAK Homolog of Xenopus MO15 Cdk activating kinase Kinase subunit of CAK MO15 MO15, Xenopus, homolog of P39 Mo15 p39MO15 Serine threonine kinase Stk1 Serine/threonine protein kinase 1 Serine/threonine protein kinase MO15 STK1 TFIIH basal transcription factor complex kinase subunit |
Fig1:
Immunocytochemistry analysis of HeLa cells labeling Cdk7 with Rabbit anti-Cdk7 antibody (ET1701-25) at 1/100 dilution. Cells were fixed in 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-Cdk7 antibody (ET1701-25) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI. Beta tubulin (M1305-2, red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594, HA1126) was used as the secondary antibody at 1/1,000 dilution. |
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Fig2: ICC staining of Cdk7 in A431 cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 1% Blocker BSA for 15 minutes at room temperature. Cells were probed with the primary antibody (ET1701-25, 1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue). | |
Fig3: ICC staining of Cdk7 in HepG2 cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 1% Blocker BSA for 15 minutes at room temperature. Cells were probed with the primary antibody (ET1701-25, 1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue). | |
Fig4: ICC staining of Cdk7 in 293 cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 1% Blocker BSA for 15 minutes at room temperature. Cells were probed with the primary antibody (ET1701-25, 1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue). |
Fig5: Flow cytometric analysis of Cdk7 was done on A431 cells. The cells were fixed, permeabilized and stained with the primary antibody (ET1701-25, 1/50) (red). After incubation of the primary antibody at room temperature for an hour, the cells were stained with a Alexa Fluor 488-conjugated Goat anti-Rabbit IgG Secondary antibody at 1/1000 dilution for 30 minutes.Unlabelled sample was used as a control (cells without incubation with primary antibody; black). |