Staining of myofibrils with fluorescent antibody against the 10S component of the original alpha-actinin preparation.

Staining of myofibrils with fluorescent antibody against the 10S component of the original alpha-actinin preparation. Research Abstract Details 

Research Abstract Table of Contents

Jump to the:

Staining of myofibrils with fluorescent antibody against the 10S component of the original alpha-actinin preparation. Abstract Text:

H Sugita,T Masaki,S Ebashi,

Staining of myofibrils with fluorescent antibody against the 10S component of the original alpha-actinin preparation. Publishing Authors By Initials

H Sugita,T Masaki,S Ebashi,

For similar animals: chordata: vertebrates: mammals: lagomorpha: rabbits research abstracts see: animals: chordata: vertebrates: mammals: lagomorpha: rabbits research

PUBMED ID PMID:

MEDLINE DATE:

Staining of myofibrils with fluorescent antibody against the 10S component of the original alpha-actinin preparation. Journal Published:

PUBLICATION TYPE: Journal Article

Journal: Journal of biochemistry

VOLUME: 75

Page Numbers: 671-3

Journal Abbreviation: J. Biochem.

ISSN: 0021-924X

DAY: 19

MONTH: Mar

YEAR: 1974

Staining of myofibrils with fluorescent antibody against the 10S component of the original alpha-actinin preparation. Information

Number of References:

LANGUAGE: eng

NlmUniqueID: 376600

Staining of myofibrils with fluorescent antibody against the 10S component of the original alpha-actinin preparation. Keywords Mesh Terms:

KEYWORDS: Rabbits

MESH TERMS: immunology

Chemical & Substance for Abstract: Staining of myofibrils with fluorescent antibody against the 10S component of the original alpha-actinin preparation. Information

Substance Name: Muscle Proteins

Registry Number: 0

Grant and Affiliation Information for Staining of myofibrils with fluorescent antibody against the 10S component of the original alpha-actinin preparation.

AFFILIATION:

Country: JAPAN

AGENCY:

GRANT:

ACRONYM:

MEDLINETA: J Biochem

REFSOURCE:

DATABASENAME:

ACCESSION NUMBER:

Number Hits: 0

Staining of myofibrils with fluorescent antibody against the 10S component of the original alpha-actinin preparation Related Publications

• "M-substance", a new protein constituting the M-line of myofibrils.
• A new simple method of preparing actin from chicken gizzard.
• A simple method of preparing actin-free myosin from smooth muscle.
• ATP-dependent Ca binding of brain microsomes.
• Alpha-actinin, a new structural protein from striated muscle. I. Preparation and action on actomyosinàtp interaction.
• Alpha-actinin, a new structural protein from striated muscle. II. Action on actin.
• Ca-releasing action of beta, gamma-methylene adenosine triphosphate on fragmented sarcoplasmic reticulum.
• Ca2+ regulation in vascular smooth muscle.
• Ca2+ regulation in vascular smooth muscle. II. Ca2+ binding of aorta leiotonin.
• Calcium-induced conformational changes and mutual interactions of troponin components as studied by spin labeling.
• Cardiac troponin.
• Crystallization and preliminary crystallographic data of chicken gizzard G-actin . DNase I complex and Physarum G-actin . DNase I complex.
• Detection of calcium binding proteins by 45Ca autoradiography on nitrocellulose membrane after sodium dodecyl sulfate gel electrophoresis.
• Does phosphorylation of myosin light chain have direct relation to regulation in smooth muscle?
• Effect of phosphates on the structure of the actin filament.
• Essential factor of gizzard "troponin" fraction. A new type of regulatory protein.
• Isolation from bovine brain of 155 kDa component exhibiting myosin light chain kinase activity.
• Localization of 6S component of a alpha-actinin at Z-band.
• Periodic distribution of troponin along the thin filament.
• Preparation of protein components exhibiting myosin light chain kinase activities from bovine aorta: discrepancies between its enzyme activity and actomyosin activating effect.
• Proceedings: Regulation of the myosin-actin interaction by the Ca2+ -troponin-tropomyosin system.
• Requirement of Ca ion for the stimulating effect of cyclic 3',5'-AMP on muscle phosphorylase b kinase.
• Reversible change in physical state of troponin induced by calcium ion.
• Reversible stimulation of muscle phosphorylase b kinase by low concentrations of calcium ions.
• Sea urchin protease specific to the SPKK motif in histone.
• Separation of troponin into its three components.
• Staining of myofibrils with fluorescent antibody against the 10S component of the original alpha-actinin preparation.
• The localization of troponin in tropomyosin paracrystals.
• Troponin and its components.
• Troponin. I. Preparation and physiological function.