[CAS NO. ]  MicroStacker™ Goat Anti-Mouse AP-Polymer

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PRODUCTS SPECIFICATIONS

Catalog
CNV-CSM1011
Brand
Celnovte

DESCRIPTION

Applications

Detection of Mouse Primary Antibodies on Human Tissue in IHC


Storage Conditions

2-8 C | 36-46 F


Technology

Micropolymer with Fab' Fragments


Format

Ready-to-Use


Product Features

 1-Step System – Simple and efficient manual workflow based on proprietary MicroStacker™ technology

 Specific Detection – Designed to detect mouse primary antibodies on human tissue with high accuracy

 Bright, High-Contrast Signal – Utilizes Fast Red substrate, providing a vivid signal with excellent contrast against background

 Rapid and Reliable – Delivers clear and sharp staining in less time compared to conventional AP polymers


Recommended Protocol

 Primary Antibody: Room temperature, 30-60 minutes

 Detection Polymer: Room temperature, 30 minutes

 Fast Red Chromogen: 6-8 minutes


Application Notes

 Ideal for Pigmented Tissues – Suitable for tissues with endogenous pigments, such as melanoma and lung cancer, ensuring clear visualization against dark backgrounds

 Multiplex Compatibility – Suitable for sequential multiplex IHC applications, allowing multiple targets to be detected on the same tissue section without cross-reactivity


MicroStacker™ Technology Platform

The MicroStacker™ Goat Anti-Mouse AP Polymer is a biotin-free, alkaline phosphatase (AP) polymer system designed for detecting mouse primary antibodies on human tissue. This advanced system incorporates Fast Red chromogen to produce high-contrast staining, even in pigmented tissues.


Celnovte’s proprietary MicroStacker™ technology employs micro-polymer scaffolds that enable directional attachment of Fab’ fragments to the poly-AP core. This design prevents antibody binding sites from being blocked during conjugation, resulting in enhanced sensitivity and minimal background interference.


The compact polymeric structure allows for deep penetration into tissue, providing uniform staining across nuclear, cytoplasmic, and membranous antigens. By eliminating endogenous biotin interference and non-specific Fc receptor binding, the system ensures exceptional specificity and reproducibility, making it ideal for challenging immunohistochemical applications and sequential multiplex IHC workflows.