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Protamine

PROTAMINE Struktur
9012-00-4
CAS-Nr.
9012-00-4
Bezeichnung:
Protamine
Englisch Name:
PROTAMINE
Synonyma:
HSDB 3251;PROTAMINE;protamines;PROTAMINE USP/EP/BP;protamine from salmon;protamine free base grade iv;Protamine from salmon Grade IV, Histone, free(Millon test);(S)-7-[[6-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-2,3-dihydro-5-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
CBNumber:
CB9468351
Summenformel:
Molgewicht:
0
MOL-Datei:
Mol file

Protamine Eigenschaften

storage temp. 
-20°C
L?slichkeit
H2O: clear

Sicherheit

WGK Germany  3
RTECS-Nr. UK9440000
Giftige Stoffe Daten 9012-00-4(Hazardous Substances Data)

Protamine Chemische Eigenschaften,Einsatz,Produktion Methoden

Chemische Eigenschaften

Water soluble, producing basic solu- tions.

Verwenden

Protamine from salmon has been used to avoid in vitro AT complex formation in samples from dogs pre-treated with heparin. It has also been used to study the influences of external potential on adsorption of various proteins to a metal surface.

Definition

protamine: Any of a group of proteinsof relatively low molecularweight found in association with thechromosomal DNA of vertebratesperm cells. They contain a singlepolypeptide chain comprising about67% arginine. Protamines are thoughtto protect and support the chromosomes.

Allgemeine Beschreibung

Protamines are proteins rich in cysteine and arginine. It possesses many phosphorylation sites. Salmon fish contains around 15 genes encoding protamine. It is found to be localized to the sperm head.

Mechanism of action

Protamine sulfate has been approved in the United States as a specific antagonist to heparin since 1968. Protamines are an arginine-rich, highly basic group of simple proteins derived from salmon sperm. The highly acidic heparin polysaccharides exhibit their anticoagulant activity through binding to antithrombin III. Because of the basicity of protamine, heparin has an increased affinity for protamine relative to antithrombin III. In fact, its binding affinity for protamine is so much greater than that of antithrombin III that protamine actually will induce dissociation of the heparin/antithrombin III complex. If protamine is administered in the absence of heparin, it can have marked effects on coagulation. Protamine is not completely selective for heparin and, in vivo, also interacts with fibrinogen, platelets, and other plasma proteins causing anticoagulation. For this reason, use of the minimal amount of protamine necessary to antagonize heparin-associated bleeding should be employed (usually 1 mg of protamine intravenously for every 100 U of heparin remaining in the patient).

Nebenwirkungen

Anaphylaxis also has been associated with the use of protamine. Although development of protamine anaphylaxis is not limited to diabetics, those patients with diabetes that have used protaminecontaining insulin (NPH or protamine zinc) do have a slightly increased risk of anaphylaxis. Some less common reactions to protamine include pulmonary vasoconstriction, hypotension, and thrombus formation.

Protamine Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Protamine Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 73)Lieferanten
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+8615604608665 15604608665
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Shijiazhuang Tongyang Import and Export Co., LTD
18031361688;
admin@sjztongyang.com China 977 58
PT CHEM GROUP LIMITED

peter68@ptchemgroup.com China 35425 58
Jiangsu Boquan Biotechnology Co., Ltd.
+86-18168774353
boquanshengwu003@boquansw.com China 248 58

9012-00-4(Protamine)Verwandte Suche:


  • protamines
  • PROTAMINE
  • protamine free base grade iv
  • protamine from salmon
  • HSDB 3251
  • PROTAMINE USP/EP/BP
  • Protamine from salmon Grade IV, Histone, free(Millon test)
  • (S)-7-[[6-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-2,3-dihydro-5-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
  • 9012-00-4
  • Biochemicals and Reagents
  • BioChemical
  • Substrate Analogs
  • Enzyme Inhibitors
  • Enzyme Inhibitors by Type
  • Enzymes, Inhibitors, and Substrates
  • Enzyme Inhibitors
  • Enzyme Inhibitors by Type
  • Substrate Analogs
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