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Mouse Cdk2 ELISA Kit

SKU:
MOFI00502
Product Type:
ELISA Kit
Size:
96 Assays
Uniprot:
P97377
Sensitivity:
0.094ng/ml
Range:
0.156-10ng/ml
ELISA Type:
Sandwich
Synonyms:
CDK2, Cell division protein kinase 2, p33 protein kinase, CDKN2, cdc2-related protein kinase, Cell division kinase 2
Reactivity:
Mouse
Research Area:
Cell Cycle
€649
Frequently bought together:

Description

system_update_altDatasheetsystem_update_altMSDS

Mouse Cdk2 ELISA Kit

The Mouse CDK2 ELISA Kit is a reliable tool for the quantitative detection of Cyclin-Dependent Kinase 2 (CDK2) levels in mouse serum, plasma, and cell lysates. This kit offers high sensitivity and specificity, ensuring accurate and reproducible results for a variety of research applications.CDK2 is an important enzyme that regulates the cell cycle and plays a key role in cell division. Dysregulation of CDK2 activity has been implicated in various diseases, including cancer and neurodegenerative disorders.

Therefore, measuring CDK2 levels can provide valuable insights into disease progression and potential therapeutic targets.With its user-friendly protocol and efficient performance, the Mouse CDK2 ELISA Kit is an essential tool for researchers studying cell cycle regulation, cancer biology, and drug development in mouse models. Trust in the reliability and precision of this kit to advance your research efforts. Visit www.assaygenie.com/mouse-cdk2-elisa-kit/ to learn more and order your kit today.

Product Name:Mouse Cdk2 ELISA Kit
Product Code:MOFI00502
Size:96 Assays
Alias:CDK2, Cell division protein kinase 2, p33 protein kinase, CDKN2, cdc2-related protein kinase, Cell division kinase 2
Detection Method:Sandwich ELISA
Application:This immunoassay kit allows for the in vitro quantitative determination of Mouse CDK2 concentrations in serum plasma and other biological fluids.
Sensitivity:0.094ng/ml
Range:0.156-10ng/ml
Storage:4°C for 6 months
Note:For Research Use Only
Recovery: Matrices listed below were spiked with certain level of Mouse CDK2 and the recovery rates were calculated by comparing the measured value to the expected amount of Mouse CDK2 in samples.
MatrixRecovery range(%)Average(%)
serum(n=5)92-10197
EDTA plasma(n=5)87-10295
UFH plasma(n=5)92-10299
Linearity:The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Mouse CDK2 and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
Sample1:21:41:8
serum(n=5)87-105%88-105%90-105%
EDTA plasma(n=5)85-101%88-98%83-98%
UFH plasma(n=5)82-94%80-97%81-91%
Intra Assay:CV <8%
Inter Assay:CV <10%
ComponentQuantityStorage
ELISA Microplate (Dismountable)8-12 strips4°C for 6 months
Lyophilized Standard24°C/-20°C
Sample/Standard Dilution Buffer20ml4°C
Biotin-labeled Antibody(Concentrated)120ul4°C (Protect from light)
Antibody Dilution Buffer10ml4°C
HRP-Streptavidin Conjugate(SABC)120ul4°C (Protect from light)
SABC Dilution Buffer10ml4°C
TMB Substrate10ml4°C (Protect from light)
Stop Solution10ml4°C
Wash Buffer(25X)30ml4°C
Plate Sealer5-

Other materials and equipment required:

  • Microplate reader with 450 nm wavelength filter
  • Multichannel Pipette, Pipette, microcentrifuge tubes and disposable pipette tips
  • Incubator
  • Deionized or distilled water
  • Absorbent paper
  • Buffer resevoir
UniprotP97377
UniProt Protein Function:CDK2: a protein kinase of the CDK family. An important component of the cell cycle machinery. Activity of CDK2 is maximal during S phase and G2. Cdk2/cyclin E kinase activity is important for the G1 to S transition and phosphorylates the Rb protein. In S-phase, active cdk2/cyclin A complexes predominate and phosphorylate E2F, and the active cdk2 complex persists in the nucleus through G2. Part of the Rb pathway disregulated in most tumors. Target of several candidate cancer drugs. However, inhibition does not always prevent cancer cell growth, possibly due to CDK redundancy. Inhibitors: BMS-265246, BMS-265246-01, R-roscovitine (CYC200, CYC202), SU9516, R547, L868276
UniProt Protein Details:

Protein type:Cell cycle regulation; Protein kinase, CMGC; Protein kinase, Ser/Thr (non-receptor); Kinase, protein; EC 2.7.11.22; CMGC group; CDK family; CDK1 subfamily; CDK/CDK1 subfamily

Cellular Component: Cajal body; chromosome, telomeric region; condensed chromosome; cyclin-dependent protein kinase holoenzyme complex; cytoplasm; cytosol; endosome; intracellular membrane-bound organelle; nucleus; transcription factor complex; X chromosome; Y chromosome

Molecular Function:cyclin binding; cyclin-dependent protein kinase activity; histone kinase activity; kinase activity; protein binding; protein complex binding; protein kinase activity

Biological Process: cellular response to insulin stimulus; centriole replication; G1/S transition of mitotic cell cycle; peptidyl-serine phosphorylation; positive regulation of cell proliferation; positive regulation of DNA replication initiation; positive regulation of transcription, DNA-dependent; potassium ion transport; protein amino acid phosphorylation; response to cAMP; response to electrical stimulus

UniProt Code:P97377
NCBI GenInfo Identifier:8039782
NCBI Gene ID:12566
NCBI Accession:P97377.2
UniProt Secondary Accession:P97377,O55105,
UniProt Related Accession:P97377
Molecular Weight:33,887 Da
NCBI Full Name:Cyclin-dependent kinase 2
NCBI Synonym Full Names:cyclin-dependent kinase 2
NCBI Official Symbol:Cdk2  
NCBI Official Synonym Symbols:A630093N05Rik  
NCBI Protein Information:cyclin-dependent kinase 2
UniProt Protein Name:Cyclin-dependent kinase 2
UniProt Synonym Protein Names:Cell division protein kinase 2
Protein Family:Cyclin-dependent kinase
UniProt Gene Name:Cdk2  
UniProt Entry Name:CDK2_MOUSE

*Note: Protocols are specific to each batch/lot. For the correct instructions please follow the protocol included in your kit.

StepProcedure
1. Set standard, test sample and control (zero) wells on the pre-coated plate respectively, and then, record their positions. It is recommended to measure each standard and sample in duplicate. Wash plate 2 times before adding standard, sample and control (zero) wells!
2.Aliquot 0.1ml standard solutions into the standard wells.
3. Add 0.1 ml of Sample / Standard dilution buffer into the control (zero) well.
4. Add 0.1 ml of properly diluted sample (Human serum, plasma, tissue homogenates and other biological fluids.) into test sample wells.
5.Seal the plate with a cover and incubate at 37 °C for 90 min.
6. Remove the cover and discard the plate content, clap the plate on the absorbent filter papers or other absorbent material. Do NOT let the wells completely dry at any time. Wash plate X2.
7. Add 0.1 ml of Biotin- detection antibody working solution into the above wells (standard, test sample & zero wells). Add the solution at the bottom of each well without touching the side wall.
8.Seal the plate with a cover and incubate at 37°C for 60 min.
9. Remove the cover, and wash plate 3 times with Wash buffer. Let wash buffer rest in wells for 1 min between each wash.
10. Add 0.1 ml of SABC working solution into each well, cover the plate and incubate at 37°C for 30 min.
11. Remove the cover and wash plate 5 times with Wash buffer, and each time let the wash buffer stay in the wells for 1-2 min.
12. Add 90 µL of TMB substrate into each well, cover the plate and incubate at 37°C in dark within 10-20 min. (Note: This incubation time is for reference use only, the optimal time should be determined by end user.) And the shades of blue can be seen in the first 3-4 wells (with most concentrated standard solutions), the other wells show no obvious color.
13. Add 50 µL of Stop solution into each well and mix thoroughly. The color changes into yellow immediately.
14. Read the O.D. absorbance at 450 nm in a microplate reader immediately after adding the stop solution.

When carrying out an ELISA assay it is important to prepare your samples in order to achieve the best possible results. Below we have a list of procedures for the preparation of samples for different sample types.

Sample Type Protocol
Serum:

If using serum separator tubes, allow samples to clot for 30 minutes at room temperature. Centrifuge for 10 minutes at 1,000x g. Collect the serum fraction and assay promptly or aliquot and store the samples at -80°C. Avoid multiple freeze-thaw cycles.

If serum separator tubes are not being used, allow samples to clot overnight at 2-8°C. Centrifuge for 10 minutes at 1,000x g. Remove serum and assay promptly or aliquot and store the samples at -80°C. Avoid multiple freeze-thaw cycles.

Plasma:

Collect plasma using EDTA or heparin as an anticoagulant. Centrifuge samples at 4°C for 15 mins at 1000 - g within 30 mins of collection. Collect the plasma fraction and assay promptly or aliquot and store the samples at -80°C. Avoid multiple freeze-thaw cycles. Note: Over haemolysed samples are not suitable for use with this kit.

Urine & Cerebrospinal Fluid:

Collect the urine (mid-stream) in a sterile container, centrifuge for 20 mins at 2000-3000 rpm. Remove supernatant and assay immediately. If any precipitation is detected, repeat the centrifugation step. A similar protocol can be used for cerebrospinal fluid.

Cell culture supernatant:

Collect the cell culture media by pipette, followed by centrifugation at 4°C for 20 mins at 1500 rpm. Collect the clear supernatant and assay immediately.

Cell lysates:

Solubilize cells in lysis buffer and allow to sit on ice for 30 minutes. Centrifuge tubes at 14,000 x g for 5 minutes to remove insoluble material. Aliquot the supernatant into a new tube and discard the remaining whole cell extract. Quantify total protein concentration using a total protein assay. Assay immediately or aliquot and store at ≤ -20°C.

Tissue homogenates:

The preparation of tissue homogenates will vary depending upon tissue type. Rinse tissue with 1X PBS to remove excess blood & homogenize in 20ml of 1X PBS (including protease inhibitors) and store overnight at ≤ -20°C. Two freeze-thaw cycles are required to break the cell membranes. To further disrupt the cell membranes you can sonicate the samples. Centrifuge homogenates for 5 mins at 5000xg. Remove the supernatant and assay immediately or aliquot and store at -20°C or -80°C.

Tissue lysates:

Rinse tissue with PBS, cut into 1-2 mm pieces, and homogenize with a tissue homogenizer in PBS. Add an equal volume of RIPA buffer containing protease inhibitors and lyse tissues at room temperature for 30 minutes with gentle agitation. Centrifuge to remove debris. Quantify total protein concentration using a total protein assay. Assay immediately or aliquot and store at ≤ -20 °C.

Breast Milk:

Collect milk samples and centrifuge at 10,000 x g for 60 min at 4°C. Aliquot the supernatant and assay. For long term use, store samples at -80°C. Minimize freeze/thaw cycles.

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