in Vitro Diagnostic Kit Raw Material Enzyme Preparation Neuraminidase, Nrh

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  • in Vitro Diagnostic Kit Raw Material Enzyme Preparation Neuraminidase, Nrh
  • in Vitro Diagnostic Kit Raw Material Enzyme Preparation Neuraminidase, Nrh
  • in Vitro Diagnostic Kit Raw Material Enzyme Preparation Neuraminidase, Nrh
  • in Vitro Diagnostic Kit Raw Material Enzyme Preparation Neuraminidase, Nrh
  • in Vitro Diagnostic Kit Raw Material Enzyme Preparation Neuraminidase, Nrh
  • in Vitro Diagnostic Kit Raw Material Enzyme Preparation Neuraminidase, Nrh
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Basic Info.

Model NO.
DS0220
EINECS
No
Classification
Biological Agents
Grade
AR
Specific Usage
For Biological Purpose
Content
Standard
Usage
Laboratory Reagents, Analytical Reagents, Diagnostic Reagents
Source
Composition
Habit Appellation
Glucose Dehydrogenase, Gdh
Application
Scientific Research, Health
Property
Biochemical Reagent
Storage
Low Temperature Storage
Use to
in Vitro Diagnostic Kit
Manufactor
Hubei New Desheng Material Technology Co., Ltd
Dosage Form
White Freeze-Dried Powder
Transport Package
Refrigerated Transport
Specification
10mg/bottle
Trademark
DeSheng
Origin
Ezhou City, Hubei Province, China
Production Capacity
50g Per Month

Product Description

Basic information
 
Dosage form: White freeze-dried powder, or liquid Molecular weight: About58 kDa (SDS-PAGE detection)
Save buffer: 50mM phosphate buffer, pH 6.8 Purity ≥ 90% (SDS-PAGE detection)
Enzyme activity: 100U/mg protein Transportation Conditions: Low temperature, ice bag
Source: Gene recombination expression Safety tips: Not applicable for human experiments
storage condition: Store at 4 ºC for about a year (after packaging according to dosage, store at -20 ºC or -80 ºC for a longer period of time and try to avoid repeated freeze-thaw)

Product Introduction

Neuraminidase (NRH, EC 3.2.1.18) is commonly known as acetylneuraminidase (sialidase). This enzyme catalyzes the hydrolysis of glycoproteins and oligosaccharides α 2-3, α 2-6 and α N-acetylneuraminic acid residues connected by 2-8 bonds.

Biochemical research

The concentration of sialic acid (SA) in the blood has been regarded as an important indicator for monitoring the presence and development of malignant tumors, and has been widely used in the diagnosis and monitoring of various tumors (such as lung cancer, gastric cancer, colorectal cancer, liver cancer, ovarian cancer, etc.). Enzymatic detection of sialic acid has the advantages of speed, simplicity, high sensitivity, and ease of automation. NRH is a very important enzyme in the sialic acid enzyme detection kit, and as the first step enzyme in initiating the entire chemical reaction of the kit, it has a very important role and significance.


in Vitro Diagnostic Kit Raw Material Enzyme Preparation Neuraminidase, Nrh


The relationship between enzyme preparations, new Trinder's reagents, and Good's buffer


There are many principles of in vitro diagnostic kits, and the most common one is a diagnostic kit based on the Trinder reaction principle (also known as enzyme method), which can be used for the detection of uric acid, creatinine, blood sugar, cholesterol, triglycerides, etc. in blood tests. This diagnostic kit typically includes important components such as enzymes, new Trinder's reagents, and Good's buffer.

By adding the new Trinder's reagent to the test substance, a color reaction occurs, and the value of the test item is calculated through absorbance measurement. For example, the values of blood sugar and uric acid in serum. The new Trinder's reagent has the advantages of high water solubility, UV absorption of color reaction products>540nm, wide pH range requirements for color reactions, and high sensitivity for color reactions.

 
in Vitro Diagnostic Kit Raw Material Enzyme Preparation Neuraminidase, Nrh
in Vitro Diagnostic Kit Raw Material Enzyme Preparation Neuraminidase, Nrh
in Vitro Diagnostic Kit Raw Material Enzyme Preparation Neuraminidase, Nrh


The use of enzyme preparations in the Trinder reaction is due to the presence of too many substances in the serum, and the specificity of enzyme preparations. For example, adding glucose oxidase will only catalyze the oxidation of blood sugar to generate hydrogen peroxide, without catalyzing the oxidation of uric acid and other substances present in the serum, ensuring the accuracy of the detection results as much as possible. However, pH value has a significant impact on enzyme activity, and each enzyme has its own high activity pH range. At this point, Good's buffer is needed to adjust the pH value.

Different Good's buffers can provide suitable buffer intervals for different enzymes. Good's buffer has the advantages of high water solubility, bottom cell membrane permeability, stable acid-base dissociation constant, low metal chelating ability, high chemical stability, etc. In summary, enzyme preparations, new Trinder's reagents, and Good's buffer complement each other in the diagnostic kit, making corresponding contributions to the precise detection of diseases.

 
in Vitro Diagnostic Kit Raw Material Enzyme Preparation Neuraminidase, Nrh
in Vitro Diagnostic Kit Raw Material Enzyme Preparation Neuraminidase, Nrh
in Vitro Diagnostic Kit Raw Material Enzyme Preparation Neuraminidase, Nrh

Company Introduction
Hubei New Desheng Material Technology Co., Ltd. specializes in the production of blood collection tube additives, chemiluminescent reagents, biological buffers, chromogenic substrates, enzyme preparations, antigen antibodies and other biochemical reagents. Founded in 2005, Desheng has a professional R&D team and advanced production equipment!

 
in Vitro Diagnostic Kit Raw Material Enzyme Preparation Neuraminidase, Nrh
in Vitro Diagnostic Kit Raw Material Enzyme Preparation Neuraminidase, Nrh
in Vitro Diagnostic Kit Raw Material Enzyme Preparation Neuraminidase, Nrh
 
in Vitro Diagnostic Kit Raw Material Enzyme Preparation Neuraminidase, Nrh
in Vitro Diagnostic Kit Raw Material Enzyme Preparation Neuraminidase, Nrh
in Vitro Diagnostic Kit Raw Material Enzyme Preparation Neuraminidase, Nrh

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