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178273 Aphidicolin - CAS 38966-21-1 - Calbiochem

Descripción

Replacement Information

Tabla espec. clave

Empirical FormulaCAS #
C₂₀H₃₄O₄ 38966-21-1

Products

Número de referenciaEmbalaje Cant./Env.
178273-1MG Ampolla de plást. 1 mg
Description
OverviewA cell-permeable tetracyclic diterpene antibiotic that acts as a cell synchronization agent. Blocks the cell cycle at early S-phase. Specific inhibitor of DNA polymerase α and δ in eukaryotic cells and in some viruses. Potentiates apoptosis induced by arabinosyl nucleosides in leukemia cell lines. Also induces apoptosis in HeLa S3 cells, but inhibits vincristine-induced apoptosis in the p53-negative human prostate cancer cell line PC-3. Also available as a 30 mM solution in DMSO (Cat. No. 504744).
Catalogue Number178273
Brand Family Calbiochem®
References
ReferencesBorner, M.M., et al. 1995. Cancer Res. 55, 2122.
Poluha, W., et al. 1995. Oncogene 10, 185.
Urbani, L., et al. 1995. Exp. Cell Res. 219, 159.
Schimke, R.T., et al. 1994. Philos. Trans. R. Soc. London. B. Biol. Sci. 345, 311.
Kuwakado, K., et al. 1993. Biochem. Pharmacol. 46, 1909.
Hubermann, J.A. 1981. Cell 23, 647.
Product Information
CAS number38966-21-1
ATP CompetitiveN
FormWhite solid
Hill FormulaC₂₀H₃₄O₄
Chemical formulaC₂₀H₃₄O₄
ReversibleN
Structure formula ImageStructure formula Image
Applications
Biological Information
Primary TargetDNA polymerase α, DNA polymerase δ
Purity≥98% by TLC
Physicochemical Information
Cell permeableY
Dimensions
Materials Information
Toxicological Information
Safety Information according to GHS
RTECSPB9185000
Safety Information
Product Usage Statements
Storage and Shipping Information
Ship Code Ambient Temperature Only
Toxicity Standard Handling
Storage +2°C to +8°C
Do not freeze Ok to freeze
Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 2 months at -20°C.
Packaging Information
Transport Information
Supplemental Information
Specifications

Documentation

Aphidicolin - CAS 38966-21-1 - Calbiochem Ficha datos de seguridad (MSDS)

Título

Ficha técnica de seguridad del material (MSDS) 

Aphidicolin - CAS 38966-21-1 - Calbiochem Certificados de análisis

CargoNúmero de lote
178273

Referencias bibliográficas

Visión general referencias
Borner, M.M., et al. 1995. Cancer Res. 55, 2122.
Poluha, W., et al. 1995. Oncogene 10, 185.
Urbani, L., et al. 1995. Exp. Cell Res. 219, 159.
Schimke, R.T., et al. 1994. Philos. Trans. R. Soc. London. B. Biol. Sci. 345, 311.
Kuwakado, K., et al. 1993. Biochem. Pharmacol. 46, 1909.
Hubermann, J.A. 1981. Cell 23, 647.

Folleto

Cargo
Caspases and other Apoptosis Related Tools Brochure
Tools and Tips for Analyzing Apoptosis
Ficha técnica

Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.

Revision15-April-2008 RFH
DescriptionA cell-permeable tetracyclic diterpene antibiotic. Cell synchronization agent. Blocks the cell cycle at the early S-phase. Specific inhibitor of DNA polymerase α and δ in eukaryotic cells and in some viruses of animal origin. Potentiates apoptosis induced by arabinosyl nucleosides in leukemia cell lines. Also induces apoptosis in HeLaS3 cells, but inhibits vincristine-induced apoptosis in the p53-negative human prostate cancer cell line PC-3.
FormWhite solid
CAS number38966-21-1
RTECSPB9185000
Chemical formulaC₂₀H₃₄O₄
Structure formulaStructure formula
Purity≥98% by TLC
SolubilityDMSO (50 mg/ml), Ethanol, or Methanol
Storage +2°C to +8°C
Do Not Freeze Ok to freeze
Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 2 months at -20°C.
Toxicity Standard Handling
Merck USA index14, 727
ReferencesBorner, M.M., et al. 1995. Cancer Res. 55, 2122.
Poluha, W., et al. 1995. Oncogene 10, 185.
Urbani, L., et al. 1995. Exp. Cell Res. 219, 159.
Schimke, R.T., et al. 1994. Philos. Trans. R. Soc. London. B. Biol. Sci. 345, 311.
Kuwakado, K., et al. 1993. Biochem. Pharmacol. 46, 1909.
Hubermann, J.A. 1981. Cell 23, 647.