
S-Vision Poly-HRP Conjugated Goat Anti-Rabbit and Mouse IgG (H+L), Ready to Use
S-Vision Poly-HRP Conjugated Goat Anti-Rabbit and Mouse IgG (H+L), Ready to Use
S-Vision Poly-HRP Conjugated Goat Anti-Rabbit and Mouse IgG (H+L), Ready to Use
Product Information
Product Name |
Cat. No. |
Spec. |
S-Vision Poly-HRP Conjugated Goat Anti-Rabbit and MouseIgG (H+L),Ready to Use |
AO-03-G1303-10ML |
10mL |
AO-03-G1303-100ML |
100mL |
Product Description
This productutilize a dextran backbone towhichmultiple HRP enzyme and antibodies molecules are conjugated. This polymer creates a highly sensitive,readily available and one-step non-biotin detection system for immunohistochemical and immunocytochemical staining.This system avoids the use of streptavidin and biotin,and therefore eliminates non-specific staining as a result of endogenous biotin..It has a wide adaptability to sample processing, reducing the variability caused by different tissue processing methods.The reagent is ready-to-use, which does not need to be diluted to obtain the best dyeing ratio, reducing experimental operation errors.
Storage and Shipping Conditions
Wet ice packs for transportation,store at2-8℃ for 12 months.
ProductContent
Component Number |
Component |
AO-03-G1303-10ML |
AO-03-G1303-100ML |
AO-03-G1303 |
S-Vision Poly-HRP Conjugated Goat Anti-Rabbit and MouseIgG (H+L),Ready to Use |
10mL |
100mL |
Product Manual |
1份 |
Staining Process
1. Manually IHCStaining
Procedures |
Reagent |
Protocol |
Dewax |
BioDewax and Clear Solution (RecommendationG1128) |
The sections were placed in BioDewax and Clear SolutionⅠ10min-BioDewax and Clear Solution Ⅱ10min-BioDewax and Clear Solution Ⅲ10min-absolute ethanolⅠ5min-absolute ethanolⅡ5min-absolute ethanol Ⅲ 5min-wash inpure water. |
Antigen Retrieval |
Citrate AntigenRetrieval Solution pH6.0(RecommendationG1202)orEDTA Antigen Retrieval Solution pH 9.0 (RecommendationG1203) |
Microwave Heating: Heating to boiling,maintain a temperature above 98℃ for 15-20 min,and cooling to room temperature; Pressurecooker heating: Heat in the pressure cooker to air injection for 2 min; Note: The repair time is also related to the fixed time and the antigen epitope,so the conditions can be explored. |
Blocking of the endogenous peroxidases |
3% Hydrogen peroxide |
Dipping orincubate at room temperature for 10min. Wash the slide in PBS (pH 7.4) on a shaker 3 times for 5min each time. |
Blocking |
BSA (RecommendationGC305010) |
The 3% BSA working solution was prepared,and the tissue was completely covered by drops,and incubated at room temperature for 30min. |
Primary antibody |
commercializationPrimary antibody |
Add aworking solution to completely cover the tissue,usually 100 μL,and incubate at 4℃ overnight or 37℃ for 2 hours. |
Secondary antibody |
S-vision poly-HRP conjugated antibody |
Drop this product until tissue is completely covered,usually 100 μL,incubated at room temperature for 20min. |
DAB staining
|
DAB Chromogenic Kit (RecommendationG1212) |
Add the prepared DAB working solution to completely cover the tissue and develop color for 5-10min. |
Hematoxylin staining |
Hematoxylin Solution(RecommendationG1004) hematoxylin differentiation solution(RecommendationG1039) hematoxylin bluing solution(RecommendationG1040) |
Thesections were directly stained into hematoxylin staining solution for 3-5 min and washed with water; then stained by hematoxylin differentiation solution for 2-5 s and washed with water; hematoxylinbluing solution for1min and washed with water. |
Dehydration andMounting |
Mounting Medium |
75% alcohol 5min-85% alcohol 5min-absolute ethanolⅠ5min-absolute ethanolⅡ5min- n-butyl alcohol 5min-xylene Ⅰ5min,Thesection were removed from xylene and mounting. |
2. Automation in IHC
This protocol uses theServicebio IHC-48histochemical instrument for reference only. For other instruments,refer to the instructions for each instrument.。
Procedures |
Reagent |
Protocol |
Dewax |
BioDewax and Clear Solution(RecommendationG1128) |
Dewax at62℃for3min,repeated three times,Wash with absolute ethanol for 3 times and wash twice with pure water. |
Antigen Retrieval |
Antigen Retrieval Solution(For histochemical instrument) |
Antigen Retrieval Solution(For histochemical instrument),Heat at 100℃ for 25 min and cool for 20 min. |
Blocking of the endogenous peroxidases |
3% Hydrogen peroxide |
Incubate at room temperature for 10min. |
Blocking |
BSA(RecommendationGC305010) |
The 3% BSA working solution was prepared,and incubated at room temperature for10min. |