rat interleukin 1β(IL-1β) elisa immunoassay kit Manual

This kit can be used to detect the content of IL-1β in rat serum, plasma, cell culture supernatant or other relevant biological fluids.


rat interleukin 1β(IL-1β) elisa immunoassay kit Manual - cover page
Brand
rat interleukin
Category
Drugs
Document type
User Manual
Language
Chinese
Pages
6
File format
PDF
File size
128 KB
Published
09 January, 2012
Updated
01 October, 2023
MD5 checksum
AEA34D073DD566A3339616CCECDCBDA2

About this manual

This manual describes the rat interleukin‑1β (IL‑1β) ELISA immunoassay kit, intended for research use only. It lists the detection range (3.12 pg/ml – 200 pg/ml), minimum detection limit (0.78 pg/ml), and specificity for native or recombinant rat IL‑1β without cross‑reaction.

The document provides detailed procedures for sample collection, reagent preparation, assay execution on a 96‑well plate, washing methods, calculation of concentrations, and safety precautions. Storage conditions for reagents and samples, as well as recommended equipment, are also included. This manual is written in Chinese.

What's inside

  • Detection Range and Sensitivity
  • Specificity
  • Reagent Storage
  • Sample Collection and Preservation
  • Reagent Preparation
  • Assay Procedure
  • Washing Methods
  • Calculation of Results
  • Precautions

Specifications

Detection range3.12 pg/ml – 200 pg/ml
Minimum detection limit0.78 pg/ml
SpecificityDetects rat IL‑1β only, no cross‑reaction with related proteins
Shelf life6 months
Assay format96‑well microplate

Frequently asked questions

What is the detection range of the rat IL‑1β ELISA kit?

The kit can measure concentrations from 3.12 pg/ml up to 200 pg/ml.

How should serum samples be stored before testing?

Serum can be kept at room temperature for 2 hours or at 4‑8 °C overnight, then centrifuged; for longer storage, freeze at –20 °C or –80 °C, avoiding repeated freeze‑thaw cycles.

How are results calculated after reading the plate?

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

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