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CytoWatch™ Endogenous Biotin Blocking Kit

Product key features

The CytoWatch™ Endogenous Biotin Blocking Kit provides an efficient two-step method for eliminating endogenous biotin interference.
  • Dual-component system: Includes streptavidin and biotin solutions to effectively block endogenous biotin
  • Enhanced signal clarity: Prevents false positives by minimizing background interference in biotin–streptavidin detection assays
  • Applications: Suitable for immunohistochemistry (IHC) and immunofluorescence assays where endogenous biotin may interfere
  • Comparable alternative: Equivalent to Thermo Scientific’s Endogenous Biotin-Blocking Kit

Product description

The CytoWatch™ Endogenous Biotin Blocking Kit is designed to reduce background signal in immunohistochemistry (IHC), immunofluorescence (IF), and other avidin–biotin based detection systems by effectively blocking endogenous biotin. Endogenous biotin is often present in cells and tissues where it can lead to nonspecific binding and false-positive staining when using biotinylated probes.

This kit includes two components: a streptavidin solution to bind all endogenous biotin molecules and a subsequent biotin solution to block unoccupied streptavidin sites. This two-step blocking strategy ensures complete suppression of background caused by endogenous biotin, enabling higher specificity and clarity in staining results. The CytoWatch™ kit is easy to use and integrates seamlessly into existing IHC and IF protocols.

Example protocol

AT A GLANCE

  1. Prepare test samples (tissue or cells).
  2. Add streptavidin working solution, incubate for 15 min at RT, then wash the samples.
  3. Add biotin working solution, incubate for 15 min at RT, then wash the samples.
  4. Biotin blocked samples are ready for downstream processing.

PREPARATION OF STOCK SOLUTIONS

Streptavidin Working Solution:

Add 100 µL Component A (Streptavidin Solution) to 900 µL PBS.

Biotin Working Solution:

Add 100 µL Component B (Biotin Solution) to 900 µL PBS.

SAMPLE EXPERIMENTAL PROTOCOL

Tissue Sections Blocking Protocol:
  1. Add streptavidin working solution.
  2. Incubate for 15 min at RT. Wash the samples.
  3. Add biotin working solution.
  4. Incubate for 15 min at RT. Wash the samples
  5. Biotin blocked samples are ready for downstream processing.
Note: This blocking buffer can be diluted in normal blocking buffer (preferably biotin-free if using serum).

References

View all 5 references: Citation Explorer
Engineering of Amphiphilic Erlotinib Analogue as Novel Nanomedicine for Non-Small Cell Lung Cancer Therapy.
Authors: Cong, Mei and Pang, Houjun and Xie, Guangxing and Li, Feifei and Li, Chunxiao and Sun, Hao and Yang, Shaoyou and Zhao, Weidong
Journal: International journal of nanomedicine (2023): 6367-6377
Specific delineation of BK polyomavirus in kidney tissue with a digoxigenin-labeled DNA probe.
Authors: Parkin, Rachael K and Boeckh, Michael J and Erard, Veronique and Huang, Meei-Li and Myerson, David
Journal: Molecular and cellular probes (2005): 87-92
The immunohistochemical detection of mismatch repair gene proteins (MLH1, MSH2, MSH6, and PMS2): practical aspects in antigen retrieval and biotin blocking protocols.
Authors: Manavis, Jim and Gilham, Peter and Davies, Ruth and Ruszkiewicz, Andrew
Journal: Applied immunohistochemistry & molecular morphology : AIMM (2003): 73-7
MOC31 immunoreactivity in primary and metastatic carcinoma of the liver. Report of findings and review of other utilized markers.
Authors: Proca, D M and Niemann, T H and Porcell, A I and DeYoung, B R
Journal: Applied immunohistochemistry & molecular morphology : AIMM (2000): 120-5
Anti-alpha-inhibin: marker of choice for the consistent distinction between adrenocortical carcinoma and renal cell carcinoma in fine-needle aspiration.
Authors: Fetsch, P A and Powers, C N and Zakowski, M F and Abati, A
Journal: Cancer (1999): 168-72
Page updated on September 11, 2025

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Storage, safety and handling

H-phraseH303, H313, H333
Hazard symbolXN
Intended useResearch Use Only (RUO)
R-phraseR20, R21, R22

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