Réactif anticorps VEGF pour l'immunohistochimie

【Product name】

IHC Antibody -- VEGF

【Packing specification】

【Intended use】

For Research use only. VEGF Antibody reagent is intended for use to qualitatively identify VEGF by microscopy in sections of FFPE tissue using immunohistochemical detection system.

【Principle】

Vascular endothelial growth factor (VEGF) is a secreted homodimeric glycoprotein belonging to the VEGF family with a role in stimulating angiogenesis and vasculogenesis. Add the primary antibody to bind the antigen on tissue sections, and then use HRP labeled secondary antibody binding primary antibody to form the secondary antibody-primary antibody-antigen complex. When DAB chromogenic solution is added, HRP reacts with enzyme substrate to produce brown insoluble reaction product, which indirectly indicating the existence of antigen. 

【Main components】

Immunoglobulin, antibody diluent

【Storage】

Store at 2～8℃ for 18 months。

【Sample requirements】

FFPE tissues are usually cut into sections as thin as 3～5μm with a microtome. These sections are then mounted onto glass slides that are coated with a tissue adhesive.

【Protocol】

1. Sample preparation：Deparaffinize the slides in xylene Ⅰ, Ⅱ, Ⅲ for 5 minutes；Transfer the slides once through 100%, 100%, 95%, 75% alcohols for 2 minutes respectively. Rinse slides with deionized water for 30 seconds.

2. Blocking：Block endogenous peroxidase activity by incubating sections in 3% H₂O₂ solution at room temperature for 5 minutes to block endogenous peroxidase activity. Rinse the slides with deionized water for 30 seconds.

3. Antigen retrieval：Heat the EDTA Antigen retrieval buffer to 100℃. Then place the slides in the boiled buffer and continue to heat for 15～20 min. Naturally cool down for 30 minutes. Rinse the sample with wash buffer.

4. Primary antibody incubation: Drain the slides. Add primary antibody to tissue, incubate at room temperature for 30 minutes. (use antibody diluent or PBS as control). Wash the slides in PBST for 2 times, 5 minutes for each time. If the Primary antibody is concentrated, please dilute it to RTU(ready to use) according to the information on packing. 

5. Secondary antibody: Drain the slides. Add secondary antibody to tissue and incubate at room temperature for 20 minutes. Wash the slides in PBST for 2 times, 5 minutes for each time.

6. DAB：Drain the slides. Add DAB to the tissue and incubate at room temperature for 5 min. Rinse slides with deionized water.

7. Hematoxylin staining：Drain the slides. Add Hematoxylin to the tissue and incubate at room temperature for 5 minutes. Rinse slides with water. Use the acid solution for differentiation. Rinse slides with water.

8. Déshydrater : déshydrater les lames dans des alcools à 75 % , 95 % et 100 %  pendant 2 minutes .  Séchez les lames. Couvrir le tissu taché avec une lamelle en utilisant un milieu de montage.

【Localisation positive 】

1.  Localisation positive :  cytoplasme .

2.  Contrôle positif :  cancer du côlon .

【Précautions 】

1.  Veuillez lire attentivement les instructions et vous familiariser avec tous les composants du kit avant utilisation. Suivez strictement les instructions pendant le fonctionnement.

2.  NE PAS utiliser le kit ou tout composant du kit après leur.

3.  Seuls les professionnels formés peuvent utiliser ce kit. Veuillez porter une blouse de laboratoire et des gants jetables appropriés lors de la manipulation des réactifs.

4.  Éviter tout contact de la peau, des yeux et des muqueuses avec les produits chimiques.

5.  NE PAS pipeter à la bouche.

6.  Les réactifs non utilisés, le kit usagé et les déchets doivent être éliminés conformément aux réglementations locales.

【Fabricant 】_

Nom de la société : Xiamen Talent Biomedical Technology Co., Ltd

Adresse : No. 3rd and 4th Floors, Building B10, No. 2068 Wengjiao Road West, BioMedical Park, Haicang District, Xiamen City, 36100 China

Tél : +86 592 6315755            

Courriel : tlsw@talentbiomedical.com                

Site Web : www.talentbiomedical.com

【 Symboles 】