Gastric Mucin

Delivery term:The date of payment from buyers deliver within days
  • Price:

    Negotiable

  • minimum:

  • Total supply:

  • Delivery term:

    The date of payment from buyers deliver within days

  • seat:

    Fujian

  • Validity to:

    Long-term effective

  • Last update:

    2022-08-01 06:22

  • Browse the number:

    282

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Company Profile
Quanzhou Haiyixing Bioengineering Co., Ltd
Contactaixin:

haiyixing(Mr.)  

Email:

telephone:

phone:

Arrea:

Fujian

Address:

No.26, Zishan Road, Kengtou Community, Jinlong Street, Licheng District, Quanzhou, Fujian

Website:

http://www.china-naturebio.com/ http://haiyixing.prescribedpoems.com/

Product details

Typical specification

    Nomenclature

 

Chinese name: 胃膜素

 

US Pharmacopoeia Name: Gastric mucin powder

 

CAS Number: 10047-33-3

Structure

Gastric mucin is A gastric acid-resistant glycoprotein extracted from porcine gastric mucosa

General Properties

 

Appearance:  white to yellowswish powder

 

Standard: according to chinese ministry of health drug standard edition 98 section II volume

6 and oue inner tandard

 

Specification : 

 

Items (Standard: USP 40)

Specifications

Description

Appearance and Odour

 White to  yellowswish powder



Viscosity

3.0

Assay

 

Mucin ratio

 73-90%


 

Purity

Loss on   drying :

Residueonignitio Lead/Pb Arsenic/As Mercury/Hg

Cadium/Cd

 

 5.0%(1054Hours)

 5.0%

0.5ppm

 0.5ppm

 0.5ppm

 0.5ppm

 0.5ppm

Microbial contamination


TAMC

NMT 10000 CFU/g

TYMC

NMT 100 CFU/g

E. Coli

Absence CFU/g

Salmonellae

Absence CFU /10g

 

 

Packaging: Net 25kg/fiber drum with inner-LDPE bag

 

Shelf life and storage: 24 months(not exceeding 30,70% RH) , in an airtight container.

4  Gastric mucin powder is a large glycoprotein which is thought to play a major role in the protection of the gastrointestinal tract from acid, proteases, pathogenic microorganisms, and mechanical trauma. In Vitro: Gastric mucin powder may be integrally involved in the mechanism of gastric mucosal injury caused by Helicobacter pylori leading to gastritis, peptic ulceration, and possibly gastric cancer[1]. Gastric mucins are classified into two types based on their histochemical properties. The first is a surface mucous cell-type mucin, secreted from the surface mucous cells. The second is found in deeper portions of the mucosa and is secreted by gland mucous cells, including mucous neck cells, cardiac gland cells, and pyloric gland cells. The unique O-glycans in gastric mucin appears to function as a natural antibiotic, protecting the host from H. pylori infection[2]. Gastric mucin may provide protection to the surface epithelium gastrointestinal tract by scavenging oxidants produced within the lumen; however, it does so at the expense of its viscoelastic properties. Both native and pronase-treated mucin effectively scavenge hydroxyl radical and that the scavenging properties are not significantly different. The effective concentration of mucin required for a 50% reduction in malondialdehyde production is 10 mg/mL for both native and pronase-treated mucin。

Gastric mucin powder may be integrally involved in the mechanism of gastric mucosal injury caused by Helicobacter pylori leading to gastritis, peptic ulceration, and possibly gastric cancer[1]. Gastric mucins are classified into two types based on their histochemical properties. The first is a surface mucous cell-type mucin, secreted from the surface mucous cells. The second is found in deeper portions of the mucosa and is secreted by gland mucous cells, including mucous neck cells, cardiac gland cells, and pyloric gland cells. The unique O-glycans in gastric mucin appears to function as a natural antibiotic, protecting the host from H. pylori infection[2]. Gastric mucin may provide protection to the surface epithelium gastrointestinal tract by scavenging oxidants produced within the lumen; however, it does so at the expense of its viscoelastic properties. Both native and pronase-treated mucin effectively scavenge hydroxyl radical and that the scavenging properties are not significantly different. The effective concentration of mucin required for a 50% reduction in malondialdehyde production is 10 mg/mL for both native and pronase-treated mucin。



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