E1850r Rat GAG ELISA Kit User Manual

The rat GAG ELISA kit is used to quantitatively measure the GAG content in rat serum, plasma, tissue homogenate, cell culture supernatant or other relevant liquids.


E1850r Rat GAG ELISA Kit User Manual - cover page
Brand
Elisa
Category
Drugs
Document type
User Manual
Language
Chinese
Pages
3
File format
PDF
File size
98 KB
Published
13 March, 2012
Updated
01 October, 2023
MD5 checksum
B4D4E67B8875DF0B00B37CD950C61E11

About this manual

This manual describes the intended applications of the rat GAG ELISA kit, which include quantitative measurement of GAG in rat serum, plasma, tissue homogenates, cell‑culture supernatants, and other related liquids. It explains the sandwich ELISA principle, reagent composition, and detailed preparation of standards and detection solutions.

The document provides a complete assay workflow: sample handling, plate loading, incubation times, washing procedures (both manual and automated), substrate development, termination, and optical density reading at 450 nm. It also covers calculation of sample concentrations, specificity notes, detection range, storage conditions, and shelf‑life information. This manual is written in Chinese.

What's inside

  • Intended Application
  • Principle of Assay
  • Reagent Composition and Preparation
  • Sample Preparation
  • Assay Procedure
  • Plate Washing Methods
  • Specificity
  • Data Calculation
  • Precautions
  • Detection Range

Specifications

Detection range1.56 ng/mL – 100 ng/mL
Storage temperature (long‑term)-20 °C
Storage temperature (frequent use)2‑8 °C
Shelf life6 months

Frequently asked questions

What types of samples can be measured with this kit?

The kit can quantify GAG in rat serum, plasma, tissue homogenate, cell‑culture supernatant, or other related liquids.

How is the standard solution prepared?

Dilute the 100 ng/mL standard stock with sample diluent to create a series of standards (100, 50, 25, 12.5, 6.25, 3.12, 1.56 ng/mL) and use 0 ng/mL as the blank.

How should the assay results be calculated?

Plot a standard curve using the log‑scaled concentration versus OD values, then determine sample concentrations from the curve and multiply by the dilution factor.

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