Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

CDC25C antibody

The Mouse Monoclonal anti-CDC25C antibody has been validated for WB. It is suitable to detect CDC25C in samples from Human, Mouse and Rat.
Catalog No. ABIN487484

Quick Overview for CDC25C antibody (ABIN487484)

Target

See all CDC25C Antibodies
CDC25C (Cell Division Cycle 25 Homolog C (S. Pombe) (CDC25C))

Reactivity

  • 115
  • 45
  • 38
  • 16
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 102
  • 15
Mouse

Clonality

  • 98
  • 19
Monoclonal

Conjugate

  • 65
  • 6
  • 5
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This CDC25C antibody is un-conjugated

Application

  • 93
  • 50
  • 38
  • 26
  • 26
  • 22
  • 16
  • 14
  • 10
  • 8
  • 6
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB)

Clone

DCS-193
  • Specificity

    This antibody reacts with CDC25C (60 kDa) on Western blotting.

    Cross-Reactivity (Details)

    Species reactivity (tested):Human, Mouse and Rat.

    Characteristics

    Synonyms: M-phase inducer phosphatase 3, Dual specificity phosphatase Cdc25C, Cell Division Cycle25C

    Purification

    Protein-A Agarose Chromatography

    Immunogen

    Human CDC25C. Remarks: Hybridoma was established by fusion of Mouse myeloma cell NS-2 with Balb/cmouse splenocyte.

    Isotype

    IgG1
  • Application Notes

    Western Blot: 10 μg/mL for chemiluminescence detection system. Positive Controls: HeLa, A431, ZR75-1, HEp-2, NIH/3T3, PC12. Detailed procedure is provided in Protocols.
    Other applications not tested.
    Optimal dilutions are dependent on conditions and should be determined by the user.

    Protocol

    SDS-PAGE & Western Blotting1) Wash the cells 3 times with PBS and suspend with 10 volume of cold Lysis buffer (50 mMTris-HCl, pH 7. 2, 250 mM NaCl, 0. 1% NP-40, 2 mM EDTA, 10% glycerol) containingappropriate protease inhibitors. Incubate it at 4°C with rotating for 30 minutes, thensonicate briefly (up to 10 seconds). 2) Centrifuge the tube at 12,000 x g for 10 minutes at 4°C and transfer the supernatant toanother tube. Measure the protein concentration of the supernatant and add the Lysisbuffer to make 8 mg/mL solution. 3) Mix the sample with equal volume of Laemmli’s sample buffer. 4) Boil the samples for 2 minutes and centrifuge. Load 10 μL of the sample per lane in a 1mm thick SDS-polyacrylamide gel for electrophoresis. 5) Blot the protein to a polyvinylidene difluoride (PVDF) membrane at 1 mA/cm2 for 1 hourin a semi-dry transfer system. (Transfer Buffer: 25 mM Tris, 190 mM glycine, 20% MeOH). See the manufacture's manual for the transfer procedure. 6) To reduce nonspecific binding, soak the membrane in 10% skimmed milk (in PBS, pH7. 2) for 1 hour at room temperature, or overnight at 4°C. 7) Incubate the membrane with primary antibody diluted with PBS, pH 7. 2 containing 1%skimmed milk as suggested in the APPLICATIONS for 1 hour at room temperature. (Theoptimal antibody concentration will depend on the experimental conditions. 8) Wash the membrane with PBS (5 minutes x 6 times). 9) Incubate the membrane with the 1: 10,000 POD-conjugated anti-mouse IgG diluted with1% skimmed milk (in PBS, pH 7. 2) for 1 hour at room temperature. 10) Wash the membrane with PBS (5 minutes x 6 times). 11) Wipe excess buffer from the membrane, then incubate it with appropriatechemiluminescence reagents for 1 minute. Remove extra reagent from the membrane bydabbing with a paper towel, and seal it in plastic wrap. 12) Expose to an X-ray film in a dark room for 5 minutes. Develop the film as usual. Theconditions for exposure and development may vary. Positive Controls for Western blotting: HeLa, A431, ZR75-1, HEp-2, NIH/3T3, PC12

    Restrictions

    For Research Use only
  • Concentration

    1.0 mg/mL

    Buffer

    PBS, pH 7.2 containing 50 % Glycerol without preservatives

    Preservative

    Without preservative

    Storage

    -20 °C

    Storage Comment

    Store the antibody undiluted at -20 °C.
    Shelf life: one year from despatch.

    Expiry Date

    12 months
  • Target

    CDC25C (Cell Division Cycle 25 Homolog C (S. Pombe) (CDC25C))

    Alternative Name

    CDC25C

    Background

    The activity of cyclin-dependent kinases is regulated by their phosphorylation status, which is controlled by the antagonistic action of CDC25 phosphatases. Three CDC25 genes are present in human cells: CDC25A, CDC25B and CDC25C. CDC25C is a ~56 kDa dual specific protein phosphatase that controls entry into mitosis by regulating the dephosphorylation of the Cdk1/cyclin B complex. Phosphorylation of Cdc25C creates a binding site for 14-3-3 protein which inhibits Cdc25C. This prevents activation of the Cdk1/cyclin B complex and prevents mitotic entry. Cdc25C is phosphorylated by checkpoint kinases throughout interphase but becomes dephosphorylated during mitosis. Cdc25C is also regulated by p53 via a p53 response element in its promoter, and it is predominantly expressed in the G2 phase of the cell cycle.Synonyms: Cell Division Cycle 25C, Dual specificity phosphatase Cdc25C, M-phase inducer phosphatase 3

    Gene ID

    995

    UniProt

    P30307

    Pathways

    Cell Division Cycle, M Phase
You are here:
Chat with us!