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Specification Sheets
Safety Data Sheet
Intended UseFor Mohs In Vitro Diagnostic Use
Summary and Explanation

The Mohs Mouse/Rabbit PolyDetector HRP Green Detection System is a, 1-step Fab micropolymeric detection system that allows for the demonstration of antigens in cryostat sections, formalin-fixed paraffin-embedded tissue and cell preparations. The Mohs PolyDetector kit has been developed using a micro-biopolymer conjugated to monomeric Fab’ immunoglobulin fractions targeting the Fc region of Mouse and Rabbit antibodies. Additionally, the biopolymer is labeled with high quality HRP for maximum sensitivity. This ensures excellent cellular penetration which generates consistent, reproducible sensitive and specific immuno detection for all types of nuclear, cytoplasmic and membranous antigens, in different types of frozen, FFPE tissues and cell preparations.

The increased sensitivity of the Mohs Mouse/Rabbit PolyDetector HRP Green Detection System allows for rapid staining procedures without compromising stain quality. The Mohs Mouse/Rabbit PolyDetector HRP Green Detection System is suitable for use with mouse IgG and IgM and rabbit primary antibodies, both monoclonal and polyclonal. The Mohs Mouse/Rabbit PolyDetector HRP Green Detection System kits are optimized for use with Bio SB TintoFast primary antibodies; however, they are universal kits and therefore should work equally well with antibodies from different vendors, as long as they are properly optimized.

PresentationThe Mohs Mouse/Rabbit PolyDetector HRP Green Detection System contains an Anti-mouse/Rabit Horseradish Peroxidase micro-biopolymer solution, an HRP Green Buffer Substrate, and an HRP Green Chromogen solution. All components are buffered with stabilizers and a non-azide anti-microbial agent.
Availability
CAT.#PRESENTATIONVOL
BSB 0310SMohs Mouse/Rabbit PolyDetector HRP Green Detection System5.0 ml
BSB 0310Mohs Mouse/Rabbit PolyDetector HRP Green Detection System15.0 ml
BSB 0311Mohs Mouse/Rabbit PolyDetector HRP Green Detection System50.0 ml
BSB 0312Mohs Mouse/Rabbit PolyDetector HRP Green Detection System100.0 ml

Mohs IHC Procedure

Specimen Preparation of Mohs Frozen Tissues

  1. Embed the specimen in OCT inside a cryostat.
  2. Cut sections at 4-5 µm and mount on a positively charged glass slide such as the Bio SB Hydrophilic Plus Slides (BSB 7028) or TintoDetector Cap Gap Plus Slides.
  3. Air dry the slide at room temperature for 2 minutes and then incubate the slide at 60 °C for 3 minutes in an incubator or dry bath.
  4. Fix in 100% acetone and air dry or fix with 10% NBF for 2 minutes at room temperature then rinse with distilled water and air dry.
  5. Frozen tissue pretreatment depends on the target of interest. Refer to product insert for primary antibody to determine appropriate pretreatment protocol.

Tissue Pretreatment Procedure for Mohs Frozen Tissues

    1. Subject tissues to epitope retrieval using Bio SB ImmunoDNA Retriever with Citrate (BSB 0020-BSB 0023), ImmunoDNA Retriever with EDTA (BSB 0030-BSB 0033) or Mohs ImmunoDigestor (BSB 0324- 0326).  It is recommended that user choose either a 5 minutes heat-induced epitope retrieval (HIER) method using a pressure cooker (BSB TintoRetriever Pressure Cooker) at 110°C, or a 1-minute proteolytic induced epitope retrieval (PIER) method (for Cytokeratins using 10% NBF fixed tissues).  Morphology is better with 10% NBF fixed tissues, especially when using proteolytic induced epitope retrieval method, however, antigen maybe easier to detect on the 100% acetone fixed tissue.
    2. Any of three HIER methods may be used:

a. TintoRetriever Pressure Cooker or Equivalent

Place tissues/slides in a staining dish or coplin jar containing the ImmunoDNA Retriever with Citrate or EDTA or TintoDeparaffinator Citrate or EDTA, and place on trivet or staining dish support in the pressure cooker. Add 1-2 inches of distilled water to the pressure cooker and turn heat to high (110-121° C). Incubate for 15 minutes. Open and immediately transfer slides to room temperature. Cool off for 5 -10 min

b. TintoRetriever PT Module or Water Bath Method

Place tissues/slides in a pre-warmed staining dish or coplin jar containing the ImmunoDNA Retriever with Citrate or EDTA TintoDeparaffinator Citrate or EDTA at 95°-99° C. Incubate for 30-60 minutes. Open immediately and transfer slides to room temperature.

c. Conventional Steamer Method

Place tissues/slides in a pre-warmed staining dish or coplin jar containing the ImmunoDNA Retriever with Citrate or EDTA, or TintoDeparaffinator Citrate or EDTA in a steamer, cover and steam for 30-60 minutes.

3. For PIER, apply Mohs ImmunoDigestor (BSB 0324- 0326) at room temperature for 1 min then wash.

IHC Detection Procedure

  1. After HIER or PIER, transfer slides to ImmunoDNA washer and let stand for 1-2 minutes.
  2. For manual staining, perform antibody incubation at ambient temperature. For automated staining methods, perform antibody incubation according to instrument manufacturer’s instructions.
  3. Wash slides with ImmunoDNA washer or DI water.
  4. Continue IHC detection protocol. Wash slides between each step with ImmunoDNA washer solution.

Abbreviated Mohs Immunohistochemical Protocol

StepMohs PolyDetector HRP Green Protocol
Primary Antibody4 min
Detection Step3 min
Substrate-Chromogen2 min
Counterstain / Coverslip0.5 min