Technical articles

Immunohistochemistry FAQ Analysis

Problem Cause Recommendation

Background is too high

The quality of the primary antibody is not high Use highly specific and high-titer primary antibodies

Background is too high

The concentration of the primary/secondary antibody is too high Reduce primary/secondary antibody concentrations

Background is too high

The sealing is not complete Increase the duration of protein blocking

Background is too high

The washing is not sufficient Increase the number and duration of washes

Background is too high

The background can be reduced by adjusting the parameters of the fluorescence microscope.

Weak or no signal

No target protein or very low expression Use cells or tissues with high expression levels

Weak or no signal

Poor cell permeability Increase the duration or concentration of the permeabilization agent

Weak or no signal

Primary/secondary antibody concentration too low Increase its concentration

Weak or no signal

Wrong secondary antibody selection (species mismatch) Use a secondary antibody that is matched to the species of the primary antibody

Fluorescent light that goes out quickly

Fluorescein itself has poor light stability due to its intrinsic properties Use a fluorescent secondary antibody with good light stability

Fluorescent light that goes out quickly

Seal with a common sealing agent Seal the film with a fluorescent quencher

Cells have spontaneous fluorescence

Glutaraldehyde is used for fixation Fluorescence quenching is performed after fixation and before fluorescent staining, such as with NaIO4, NaBH4, glycine, etc., and the level of autofluorescence is checked before staining

Cells have spontaneous fluorescence

The material itself (e.g., paraffin) has autofluorescence Set up a negative control to eliminate background staining by reducing the parameters of the fluorescence microscope

Cells have spontaneous fluorescence

The content of molecules (e.g., riboflavin, cytochrome) in the cell components that can produce autofluorescence is high; the ratio of dead cells/live cells in the cultured cells is high


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Categories: Technical articles
Explore topics: Immunofluorescence

Da — when not otherwise indicated, molecular weight units are daltons.   Mw — weight-average molecular weight.   Mn — number-average molecular weight.

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Cite this article

Aladdin Scientific. "Immunohistochemistry FAQ Analysis" Aladdin Knowledge Base, updated Oct 24, 2024. https://www.aladdinsci.com/us_en/faqs/immunohistochemistry-faq-analysis-en.html
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