Literature DB >> 14824487

Methyl green. III. Reaction with desoxyribonucleic acid, stoichiometry, and behavior of the reaction product.

N B KURNICK, M FOSTER.   

Abstract

1. Methyl green ("ethyl green") C. I. Number 685 was examined and found to behave identically with methyl green C. I. Number 684 (no longer available) in respect to molar extinction coefficient, effect of combination with polymerized DNA, failure to react with depolymerized DNA, and effect of pH. 2. The mass law permits the calculation of P/dye. This is found to be 13 P/dye. The same value is obtained when an excess of methyl green is caused to fade by adjusting the pH to 7.5. 3. The compound formed by methyl green with DNA has the same maximum absorption at 642.5 to 645 mmicro in the pH range 3.5-7.8, whereas the free dye fades markedly above pH 5.0.

Entities:  

Keywords:  METHYL GREEN; NUCLEIC ACIDS

Mesh:

Substances:

Year:  1950        PMID: 14824487      PMCID: PMC2147252          DOI: 10.1085/jgp.34.2.147

Source DB:  PubMed          Journal:  J Gen Physiol        ISSN: 0022-1295            Impact factor:   4.086


  3 in total

1.  Methyl green-pyronin; basis of selective staining of nucleic acids.

Authors:  N B KURNICK
Journal:  J Gen Physiol       Date:  1950-01-20       Impact factor: 4.086

2.  Crystalline desoxyribonuclease; digestion of thymus nucleic acid; the kinetics of the reaction.

Authors:  M KUNITZ
Journal:  J Gen Physiol       Date:  1950-03       Impact factor: 4.086

3.  Methyl green-pyronin; stoichiometry of reaction with nucleic acids.

Authors:  N B KURNICK; A E MIRSKY
Journal:  J Gen Physiol       Date:  1950-01-20       Impact factor: 4.086

  3 in total
  10 in total

1.  Rapid method for the detection of DNase of campylobacters.

Authors:  M L Hänninen
Journal:  J Clin Microbiol       Date:  1989-09       Impact factor: 5.948

2.  On the mechanism of the methyl green-pyronin stain for nucleic acids.

Authors:  J E Scott
Journal:  Histochemie       Date:  1967

Review 3.  [New approaches in cytometry in the field of cancer research, general biology and pathology].

Authors:  H G Schiemer
Journal:  Klin Wochenschr       Date:  1967-04-15

4.  Inhibition of pyrimidine dimer formation in DNA by cationic molecules: role of energy transfer.

Authors:  B M Sutherland; J C Sutherland
Journal:  Biophys J       Date:  1969-08       Impact factor: 4.033

Review 5.  Energy transfer and binding competition between dyes used to enhance staining differentiation in metaphase chromosomes.

Authors:  E Sahar; S A Latt
Journal:  Chromosoma       Date:  1980       Impact factor: 4.316

6.  A fast, low cost, and highly efficient fluorescent DNA labeling method using methyl green.

Authors:  Daniel Prieto; Gonzalo Aparicio; Pablo E Morande; Flavio R Zolessi
Journal:  Histochem Cell Biol       Date:  2014-03-27       Impact factor: 4.304

7.  Methyl green is a substitute for distamycin A in the formation of distamycin A/DAPI C-bands.

Authors:  T A Donlon; R E Magenis
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

8.  [Coplanar hetero-oligobases (phthalanilides), highly effective cytostatics].

Authors:  H M Rauen; K Norpoth; W Unterberg; H Haar
Journal:  Experientia       Date:  1965-05-15

9.  Simultaneous production of R-bands and either replication patterns or sister chromatid differentiation.

Authors:  P M Kroisel; W Rosenkranz; D Schweizer
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

10.  An analysis of the inactivation of the frog sperm nucleus by toluidine blue.

Authors:  R BRIGGS
Journal:  J Gen Physiol       Date:  1952-05       Impact factor: 4.086

  10 in total

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