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GB/T 23195-2008Method for the determination of catalase in bee pollen - Ultaraviolet spectrophotometry (English PDF)

蜂花粉中过氧化氢酶的测定方法 紫外分光光度法

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Issued by

SAMR; SAC

Level / Type

National · Recommended

Issue date

December 31, 2008

Implementation date

June 1, 2009

Scope

GB/T 23195-2008 is the English-translated version of 蜂花粉中过氧化氢酶的测定方法 紫外分光光度法.

GB/T 23195-2008 is the Chinese standard "Method for the determination of catalase in bee pollen - Ultaraviolet spectrophotometry". Its scope clause reads: This standard specifies the method for determination of bee pollen of catalase.

This standard is applicable by measuring catalase in bee pollen. Its clauses include reagents; equipment; preparation of test solution.

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Document preview — GB/T 23195-2008

National Standard of the People's Republic of China

ICS
65.140
Classification
B 47

Issued by: State Administration for Market Regulation; Standardization Administration of the PRC

Contents

  • 1 Scope
  • 2 Normative references
  • 4 Reagents
  • 5 Equipment
  • 6 Preparation of test solution

1 Scope

This standard specifies the method for determination of bee pollen of catalase.

This standard is applicable by measuring catalase in bee pollen.

2 Normative references

The following documents contain provisions which, through reference in this standard and become the standard terms. For dated references, subsequent

Amendments (not including errata content) or revisions do not apply to this standard, however, encourage the parties to the agreement are based on research

Whether the latest versions of these documents. For undated reference documents, the latest versions apply to this standard.

GB/T 6682 analytical laboratory use specifications and test methods (GB/T 6682-2008, ISO 3696. 1987, MOD)

Principle 3

Hydrogen peroxide absorbs strongly at a wavelength of 240nm, catalase can decompose hydrogen peroxide, the reaction solution in a certain range of absorbance

Inner circle with the reaction time reduced, can be determined according to the rate of change in absorbance measured catalase activity.

4 Reagents

Unless otherwise indicated in the analysis using only analytical reagent and in line with GB/T 6682 requirements distilled or deionized water.

4.1 phosphate buffer

pH 6.8 to 7.0, at a concentration of 50mmol/L, containing 1mmol/L disodium ethylenediamine tetraacetate (EDTA).

Weigh accurately 17.91gNa2HPO4 · 12H2O add distilled water and diluted to 500mL, as solution A;

Weigh accurately 7.80gNaH2PO4 · 2H2O add distilled water and diluted to 500mL, as solution B;

The exact amount of fluid and take 55.0mLA 45.0mLB liquid in 200mL beaker, 0.07gEDTA, add distilled water mixed

Even (added to about 150mL), calibrated to 6.8 to 7.0 with a pH meter, transferred to 200mL volumetric flask, dilute to volume, and mix.

4.2 hydrogen peroxide solution

volume fraction of 0.1%.

Imbibe 0.5mL30% hydrogen peroxide is placed 50mL brown volumetric flask, with phosphate buffer (4.1) to volume, mix,

Accurately taken from the triangular 10.0mL in 100mL Erlenmeyer flask (dark), and then accurately weighed 20.0mL phosphate buffer solution (4.1) was added to the mixed

Even that was.

4.3

liquid nitrogen.

5 Equipment

5.1

UV spectrophotometer.

5.2

refrigerated centrifuge.

5.3

constant temperature water bath.

5.4

pH meter.

5.5 Analysis of balance

a sense of the amount of 0.1mg.

5.6 pipette

100µL, 5000µL.

6 Preparation of test solution

Weigh 1g sample to the nearest 1mg, has been placed with the right amount of liquid nitrogen ice-cold porcelain mortar while adding liquid nitrogen side grinding, the sample to be fully RESEARCH […]

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This preview omits tables, figures, formulas and parts of the technical clauses. The complete document — 15 pages — is available in the English PDF.

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