#151285

Anti-RAP1 [RAP1 4C8/1]

Cat. #151285

Anti-RAP1 [RAP1 4C8/1]

Cat. #: 151285

Sub-type: Primary antibody

Unit size: 100 ug

Availability: 3-4 weeks

Target: RAP1

Class: Monoclonal

Application: ELISA ; FACS ; IHC ; IF ; WB

Reactivity: Human ; Mouse

Host: Mouse

£300.00

This fee is applicable only for non-profit organisations. If you are a for-profit organisation or a researcher working on commercially-sponsored academic research, you will need to contact our licensing team for a commercial use license.

Contributor

Inventor: Stephen West

Institute: Cancer Research UK, London Research Institute: Clare Hall Laboratories

Tool Details
Target Details
Applications
Handling
References

Tool Details

*FOR RESEARCH USE ONLY (for other uses, please contact the licensing team)

  • Name: Anti-RAP1 [RAP1 4C8/1]
  • Research fields: Cell biology;Genetics
  • Clone: RAP1 4C8/1
  • Tool sub type: Primary antibody
  • Class: Monoclonal
  • Conjugation: Unconjugated
  • Strain: Balb/c
  • Reactivity: Human ; Mouse
  • Host: Mouse
  • Application: ELISA ; FACS ; IHC ; IF ; WB
  • Description: Rap1 is a telomeric protein. Rap1 contributes to both telomere length regulation and telomere silencing.
  • Immunogen: Human Rap1
  • Isotype: IgG2b
  • Myeloma used: Sp2/0-Ag14
  • Recommended controls: HeLa cell and mouse testis extracts.

Target Details

  • Target: RAP1
  • Tissue cell line specificity: HeLa cell and mouse testis extracts.
  • Target background: Rap1 is a telomeric protein. Rap1 contributes to both telomere length regulation and telomere silencing.

Applications

  • Application: ELISA ; FACS ; IHC ; IF ; WB

Handling

  • Format: Liquid
  • Concentration: 0.43 mg/ml
  • Unit size: 100 ug
  • Storage buffer: PBS with 0.02% azide
  • Storage conditions: -15° C to -25° C
  • Shipping conditions: Dry ice

References

  • Wang et al. 2015. Circulation. 132(20):1909-19. PMID: 26416809.
  • Bombarde et al. 2010. EMBO J. 29(9):1573-84. PMID: 20407424.
  • TRF2/RAP1 and DNA-PK mediate a double protection against joining at telomeric ends.

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