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Recombinant CDK2 Monoclonal Antibody

Uniprot : P24941
  • Cat.No.:E-AB-81426

  • Host: Rabbit
  • Reactivity: H,R,Hm
  • Applications: WB,IHC-P,IF

To Purchase E-AB-81426

Size:
  • 50μL
  • 100μL
Price: $160
Qty:

Test Application

  • Verified Samples

    Reactivity Application
    Human WB
    (Jurkat,Hela,)

    Western blot detection of CDK2 in Jurkat,C6,CHO-K1,Hela cell lysates using CDK2 Rabbit mAb(1:1000 diluted).Predicted band size:34kDa.Observed band size:34kDa.

    Western blot detection of CDK2 in Jurkat,C6,CHO-K1,Hela cell lysates using CDK2 Rabbit mAb(1:1000 diluted).Predicted band size:34kDa.Observed band size:34kDa.

    IHC
    (tonsil,)

    Immunohistochemistry of Cdk2 in paraffin-embedded Human tonsil using Cdk2 Rabbit mAb at dilution 1:100

    IF
    (Hela,)

    Immunofluorescence of CDK2(green) in Hela cells using CDK2 Rabbit mAb at dilution 1:200, and DAPI(blue)

    Rat WB
    (C6,)

    Western blot detection of CDK2 in Jurkat,C6,CHO-K1,Hela cell lysates using CDK2 Rabbit mAb(1:1000 diluted).Predicted band size:34kDa.Observed band size:34kDa.

  • Dilution

    WB 1:1000-1:2000 IHC 1:50-1:100 IF 1:20-1:100

Preparation of protein samples

1.Protein extraction

1)For tissue sample
a. Take the samples, wash the tissue thoroughly with pre-cooled PBS (0.01 M, pH=7.4)(Cat# E-BC-R187) to remove the surface blood and internal debris.
b. Weigh and smash the tissue, add an appropriate ratio of RIPA Lysis Buffer (Cat# E-BC-R327)(add 10 μL PMSF and 10 μL Na3VO4 to each 1 mL RIPA Lysis) and homogenizely lyse the tissue.
It is recommended to homogenize according to the ratio of tissue weight: RIPA volume = 3:10. For example, add 1 mL RIPA Lysis Buffer to 0.3 g tissue sample, the specific volume can be adjusted according to experimental requirements.
c. Shake and lyse on the ice for 30 min after homogenization. And then sonicate the sample for 1 min (under ice water bath conditions) with 2 s’ sonication and 2 s’ intervals to make cells fully lysis and reduce the viscosity of sample.
d. Centrifuge at 12,000 rpm for 10 min at 4℃.
e. Take the supernatant and measure the protein concentration mentioned in step2.

2)For cell sample
a. Collect the cells, wash them thoroughly with pre-cooled PBS (0.01 M, pH=7.4) to remove the medium off (it is generally recommended to wash 3 times).
b. Add an appropriate ratio of RIPA Lysate Buffer (10 μL PMSF and 10 μL Na3VO4 in each 1 mL RIPA Lysis) and lyse on the ice for 30 min.
It is recommended to add 0.1 mL of RIPA Lysis Buffer to each well of a 6-well plates (the protein content in different cells may vary, and the volume of the lysate added can be appropriately adjusted).
c. Sonicate the sample for 1 min (under ice water bath conditions) with 2 s’ sonication and 2 s’ intervals to make cells fully lyse and reduce viscosity of sample.
d. Centrifuge at 12,000 rpm for 10 min at 4℃.
e. Take the supernatant and measure the protein concentration mentioned in step2.

2.Measurement of protein concentration
By the BCA method (see the Total Protein Colorimetric Assay Kit (Cat# E-BC-K318) instructions).

3.Boiling the samples
Adjust the protein concentration with PBS Buffer. Add 5 × SDS Loading Buffer (Cat# E-BC-R288) with the ratio of the protein sample: 5 × SDS Loading Buffer = 4:1 and boil the mixture for 10 min. Centrifuge at 12,000 rpm for 2 min and collect the supernatant. The denatured protein can be employed to Western Blot experiments or stored at -20℃ or -80℃.

Note: It is recommended that the total protein loading amount of test sample is about 50 μg in each well. Try to make the loading volume of each sample close to 10 μL.

Electrophoresis

1.According to the molecular weight of the target protein, prepare 0% separation gel. Add the test sample to each well, and add 5 μL of Pre-stained Protein Marker (Cat# E-BC-R273)to a reserved well in order to verify the target molecular weight and the extent of membrane transfer. Add Electrophoresis Buffer ( Cat# E-BC-R331) and start electrophoresis.

2.Electrophoresis at 80v when the samples are in stacking gel, then convert to 120v when the blue flow into the separating gel. Electrophoresis time is about 2-3 h till bromophenol blue reaches the bottom of the gel.

Transfer Membrane

1.Choose the PVDF Membrane (Cat# E-BC-R266) with a pore size of μm according to the molecular weight of the target protein. Soak the PVDF Membrane in methanol for 1 min to activate it, and then soak the PVDF Membrane in the Transmembrane Buffer (Cat# E-BC-R333), the filter paper and fiber mat must be soaked in the Transmembrane Buffer for use too.

2.Follow manufacture instructions of Transfer System for wet, semi-dry, or dry transfer.

Incubation of antibodies

1.Soak the PVDF Membrane with TBST Buffer (Cat# E-BC-R335) containing 5% Skim Milk Powder as blocking buffer and block the membrane at room temperature for .

2.According to the recommended primary antibody dilution ratio, use the TBST Buffer containing 5% Skim Milk Powder to dilute the CDK2 Antibody at , soak the PVDF Membrane in the primary antibody working solution, incubate overnight at 4 ℃, and gently shake.

3.Wash the PVDF Membrane with TBST Buffer for .

4.According to the recommended secondary antibody dilution ratio, use a TBST Buffer solution containing 2% Skim Milk Powder to dilute Goat Anti-Rabbit IgG (H+L) (peroxidase/HRP conjugated) (Cat# E-AB-1003) at . Incubate at room temperature for 1 h on a shaker.

5.Wash the PVDF Membrane with TBST Buffer for .

Detection

1.Mix A and B in the Excellent Chemiluminescent Substrate Detection kit (Cat# E-BC-R347) at the ratio of 1:1 as working solution.

2.Take out the PVDF Membrane from TBST Buffer and absorb the liquid with the filter paper. Pave the PVDF Membrane on the detection machine, add ECL working solution continuously on the PVDF Membrane, discharge the bubble and detect the result.

3.Adjust the contrast and the exposure time to get the best image.

Appendix

Product Details

Clonality Rabbit Monoclonal
Isotype IgG
Concentration 300 μg/mL
Storage Store at -20℃. Avoid freeze / thaw cycles.
Buffer 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.01% Sodium azide and 0.05% protective protein
Purification Method Affinity Purified
Research Areas Cancer, Cell Biology, Epigenetics and Nuclear Signaling
Clone No. R04-1D5
Conjugation Unconjugated

Immunogen Details

Immunogen A synthetic peptide of human Cdk2
Abbre CDK2
Synonyms Cdc2 related protein kinase,cdc2-related protein kinase,CDC28,CDC2A,Cdk 2,CDK1,CDK2,CDK2,CDKN2,Cell devision kinase 2,Cell division protein kinase 2,Cyclin dependent kinase 2,cyclin dependent kinase 2-alpha,Cyclin-dependent kinase 2,kinase Cdc2,MPF,p33 protein kinase,p33(CDK2),Recombinant Rabbit mAb,Recombinant Rabbit Monoclonal Antibody
Swissprot P24941
Gene ID 1017
Calculated MW 34kDa
Observed MW 34kDa
Cellular Localization Cytoskeleton,centrosome,Cytosol,Endosome,Nucleus,Cajal body,nucleoplasm,nucleus,Other locations:chromosome, telomeric region,condensed chromosome,cyclin A1-CDK2 complex,cyclin A2-CDK2 complex,cyclin E1-CDK2 complex,cyclin E2-CDK2 complex,cyclin-dependent protein kinase holoenzyme complex,cytoplasm,transcription factor complex,X chromosome,Y chromosome

Background

CDK2(Cyclin-dependent kinase 2) is also named as CDKN2 and belongs to the protein kinase superfamily,CMGC Ser/Thr protein kinase family,CDC2/CDKX subfamily.It is involved in the control of the cell cycle; essential for meiosis,but dispensable for mitosis.It has 2 isoforms produced by alternative splicing.

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