Mitomycin C, cell culture reagent, 2 mg

Product Description

Mitomycin C

Application Notes

Mitomycin C is the most widely used as Mitomycin antibiotics because it is the least toxic and with the most potent antitumor activity. It has extraordinarily strong activity against Ehrlich ascites tumor cells.It also possesses strong bactericidal action against Gram-positive and Gram-negative organisms and acid-fact bacilli. Mitomycin C is used to generate mitotically inactive feeder cells used in cell culture systems, such as mitotically inactive fibroblast used in embryonic stem cell (ESC) systems.

Usage Statement

Research Use Only (RUO). Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

Key Applications

Generate mitotically inactive feeder cells

Specifications

SKU	0219453202
Alternate Names	Ametycin; 7-Amino-9-a-methoxymitosane; Mit-C; Mitocin-C; Mitomycinum; Mutamycin; Azirizino[2', 3': 3,4] pyrrolo [1,2-a] indole 4,7-dione-6-amino-1,1a, 2, 8, 8a, 8b-hexahydro- 8- (hydroxymethyl) 8a-methoxy-5-methyl carbamate
Application Notes	Mitomycin C is the most widely used as Mitomycin antibiotics because it is the least toxic and with the most potent antitumor activity. It has extraordinarily strong activity against Ehrlich ascites tumor cells.It also possesses strong bactericidal action against Gram-positive and Gram-negative organisms and acid-fact bacilli. Mitomycin C is used to generate mitotically inactive feeder cells used in cell culture systems, such as mitotically inactive fibroblast used in embryonic stem cell (ESC) systems.
Base Catalog Number	19453202
Beilstein Registry Number	7231816
Biochemical Physiological Actions	Mode of Action: This product is an alkylating agent that specifically targets the guanine nucleoside sequence 5'-CpG-3'. It inhibits DNA synthesis by covalently reacting with DNA, forming crosslinks between complementary strands of DNA. This interaction prevents separation of complementary DNA strands, inhibiting DNA replication.Antimicrobial Spectrum: Mitomycin C has strong antitumor activity, especially against Ehrlich ascites tumor cells, and strong bactericidal action against gram-positive and gram-negative bacteria.
Boiling Point	534 °C
CAS #	50-07-7
EC Number	200-008-6
Grade	Cell Culture Grade
Hazard Statements	H302-H351
Melting Point	Above 680° F (EPA, 1998)
Molecular Formula	C15H18N4O5
Molecular Weight	334.332 g/mol
Pack Size	2 mg
RTECS Number	CN0700000
Safety Symbol	GHS07, GHS08
Solubility	Soluble (NTP, 1992)
Usage Statement	Research Use Only (RUO). Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.