[Manual] MicroStacker™ Polymer Detection Kit Universal, 1 Step

MicroStacker™ Polymer Detection System Universal is a biotin-free, polymeric horseradish peroxidase (HRP)- secondary antibody conjugate system for the detection of mouse and rabbit primary antibody on formalin-fixed, paraffin-embedded (FFPE) tissues in an immunohistochemistry (IHC) procedure. The innovative MicroStacker™ technology allows well-controlled layered stacking of antibodies and peroxidase enzymes on a micro-polymer scaffold. This technique results in a compact polymeric structure that easily penetrates to all cellular compartments, which provides superior sensitivity compared to other conventional HRP polymers with bulky dextran backbones. Plus, the system utilizes F(ab’) fragments of IgG secondary antibody instead of the whole IgG, which avoids the background caused by non-specific binding of whole IgG to endogenous Fc receptors.

[Manual] MicroStacker™ Polymer Detection Kit Universal, 1 Step
[Manual] MicroStacker™ Polymer Detection Kit Universal, 1 Step
[Manual] MicroStacker™ Polymer Detection Kit Universal, 1 Step
[Manual] MicroStacker™ Polymer Detection Kit Universal, 1 Step
[Manual] MicroStacker™ Polymer Detection Kit Universal, 1 Step
[Manual] MicroStacker™ Polymer Detection Kit Universal, 1 Step
[Manual] MicroStacker™ Polymer Detection Kit Universal, 1 Step
[Manual] MicroStacker™ Polymer Detection Kit Universal, 1 Step

Recommended Protocol

Deparaffinization

Deparaffinize slides in xylene, then hydrate through graded alcohols to water.

Peroxidase Blocking

Apply Peroxidase Blocking Reagent for 5 minutes. Wash twice with wash buffer for 5 minutes each.

Antigen Retrieval

Perform antigen retrieval according to the primary antibody datasheet.

Primary Antibody

Apply approximately 100 μL, or sufficient volume to cover the tissue section. Incubate for 30 to 60 minutes at room temperature. Wash twice with wash buffer for 5 minutes each.

Detection Polymer

Apply approximately 100 μL of Anti-Mouse/Rabbit HRP-Polymer, or sufficient volume to cover the tissue section. Incubate for 30 minutes at room temperature. Wash twice with wash buffer for 5 minutes each.

DAB Development

Prepare the DAB working solution by mixing DAB Chromogen with DAB Substrate Buffer at a 1:20 ratio. Use approximately 100 μL per slide. Incubate for 5 minutes at room temperature, then rinse with deionized water.

Counterstaining

Counterstain with hematoxylin, then rinse with deionized water.




Specification

DAB Substrate Buffer

Code

Product Name

Components

Specification

SD3001DAB Chromogen KitDAB Substrate (20x)1000test/box
Substrate Buffer2000test/box

SD3100

MicroStackerTM Polymer Detection Kit, Universal (3 Components)

MicroStackerTM Anti-Mouse/Rabbit HRP-Polymer

100ml(1000T)

20*DAB Chromogen

5ml

DAB Substrate Buffer

100ml

MicroStackerTM Anti-Mouse/Rabbit HRP-Polymer

30ml (300T)

20*DAB Chromogen

1.5ml

DAB Substrate Buffer

30ml

MicroStackerTM Anti-Mouse/Rabbit HRP-Polymer

10ml (100T)

20*DAB Chromogen

1ml

DAB Substrate Buffer

10ml

SD3101MicroStacker™ Polymer Detection Kit, Universal (4 components)Peroxidase Block1000test/box
Anti-Mouse/Rabbit HRP-Polymer
DAB Chromogen (20x)2000test/box
DAB Substrate Buffer
SD3102MicroStacker™ Polymer Detection Kit, Universal (5 components)Peroxidase Block1000test/box
Anti-Mouse/Rabbit HRP-Polymer
DAB Chromogen (20x)2000test/box
DAB Substrate Buffer
Hematoxylin



  • Recommended Protocol

  • Specification

Related Product

Tel

Tel

4014414689
Email

Email

info@celnovte.com
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