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AB93682

Antigen Retrieval Buffer (100X Tris Buffer, pH 10.0)

Antigen Retrieval Buffer (100X Tris Buffer, pH 10.0)

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Antigen retrieval buffer (100X Tris, pH 10.0) (ab93682) is used in heat-induced antigen retrieval (HIER) to enhance staining on formalin-fixed, paraffin-embedded tissue sections with our primary antibody range during IHC.

- Provided in 100X solution for easy dilution preparation
- Available in different formats to fit your experimental needs. Larger volume format available upon request.
- Compatible with our Lab essentials staining workflow offering
1 Images
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Antigen Retrieval Buffer (100X Tris Buffer, pH 10.0) (AB93682)
  • IHC-P

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Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Antigen Retrieval Buffer (100X Tris Buffer, pH 10.0) (AB93682)

ab93682 Antigen Retrieval Buffer 100X Tris Buffer, pH 10

Key facts

アプリケーション

IHC-P

applications

製品の状態

Liquid

form

バッファー組成

pH: 11 - 12 Constituents: 98.5% Tris buffer, 1.5% 2-butoxyethanol

storage-buffer

Reactivity data

{ "title": "Reactivity Data", "filters": { "stats": ["", "Reactivity", "Dilution Info", "Notes"] }, "values": { "IHC-P": { "reactivity":"TESTED_AND_REACTS", "dilution-info":"", "notes":"<p></p>" } } }

製品の詳細

Antigen Retrieval Buffer (100X Tris Buffer, pH 10.0) is a special solution that enables rehydrate and target retrieval in formalin-fixed, paraffin-embedded tissue sections in one step. It is optimal for use with primary antibodies that require Tris buffer (pH=10.0) pretreatment.

This product contains detergent for emulsification of the paraffin.

1X Dilution: The 100X stock solution should be diluted 100-fold with distilled water before use.

PROTOCOL:

  1. Place slides in a Coplin jar containing 1x Target Retrieval Buffer; cover with a vented plastic wrap and place the jar in microwave and set high power to boil and set low power to keep it boiling for 10 min. Let the sections cool in the microwave for at least 20min.
  2. Wash sections with hot tap water for 1 minute.
  3. Wash sections in buffer for 2x3 minutes.
  4. Block endogenous peroxidase as usual.
  5. Wash sections in buffer for 2x3 minutes.
  6. Block non-specific sites with a Blocking reagent as usual.
  7. Place optimally diluted primary antibody on the sections (incubation time and temperature for a given set of experimental conditions should be determined by the investigator).
  8. Wash sections in buffer for 2x3 minutes
  9. Rest of the procedure is same as routinely performed in your laboratory.

Other kits and reagents for IHC

Other antigen retrieval buffers include: Citrate buffer pH 6.0 ab93678, EDTA buffer pH 8.0 ab93680, Tris-EDTA buffer pH 9.0 ab93684 or see the full list of antigen retrieval buffers and enzymes.

Find more kits and reagents for antigen retrieval, blocking, signal amplification, visualization, counterstaining, and mounting in the IHC kits and reagents guide.

出荷温度及び保存条件

出荷温度
Ambient - Can Ship with Ice
短期保存温度
Ambient
長期保存温度
Ambient

製品プロトコール

ターゲットの情報

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