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Four Color Multiplex Fluorescent Immunostaining Kit (Anti Rabbit)

Four Color Multiplex Fluorescent Immunostaining Kit (Anti Rabbit)

Please note that the price mentioned above is only for your reference. To get detailed pricing information, please contact our seller, Vecent. It's important to get in touch with them to clarify any queries you may have regarding the price. Don't rely solely on the information provided in the...

Description

SKU-Pack SizeAvailabilityPrice
abs50028-20T1-2 weeks$845.00
abs50028-100T1-2 weeks$3214.00

Please note that the price mentioned above is only for your reference. To get detailed pricing information, please contact our seller, Vecent. It's important to get in touch with them to clarify any queries you may have regarding the price. Don't rely solely on the information provided in the earlier statement. Instead, reach out to our seller Vecent for further information about pricing.


Description
Description

The cellular composition of the tissue microenvironment is intricate, and the biological and clinical significance of these cells lies in their phenotype, state, abundance, and distribution. It can be shown in situ by antibody staining.Immunohistochemical staining is a widely used technique that enables researchers to study tissue morphology and protein expression in situ. Unfortunately, conventional IHC detection only allows for the visualization of a single indicator, making it challenging to accurately depict the cellular composition, status, and relationships present in the complex tissue microenvironment. This limitation can impair the ability to diagnose and treat diseases effectively.

The tyroammonia signal amplification technology is based on the same principle as the conventional immunohistochemistry DAB color rendering method. In this technology, an HRP labeled secondary antibody is utilized. The HRP enzyme facilitates the addition of a fluorescepin substrate to the system, leading to the production of an activated fluorescent substrate. Subsequently, this activated substrate binds covalently with the tyrosine present on the antigen, resulting in a stable covalent binding of fluorescepin on the sample. By rearranging the information provided, I have generated a similar content that maintains the key details of the original text.Following this, the bound antibodies were eliminated by hot repair, and a subsequent round of incubation was carried out with another primary antibody along with a distinct luciferase substrate, allowing for the possibility of multiple labeling. This method was utilized to achieve a comprehensive analysis of the sample, where various antigens were targeted and visualized simultaneously. The non-covalent binding of the antibodies allowed for gentle and specific interactions without altering the morphology and integrity of the sample. Overall, this technique provided a robust and efficient approach for studying complex biological specimens with high resolution and accuracy.

Applications
Immunohistochemical staining is primarily employed on paraffin-embedded sections of human or mouse tissues, as well as TMA chips.
Usage
To dilute fluorescent dye for signal amplification reactions, there are two methods depending on the dye form. If the dye is in dry powder form, dissolve it with 100ul of DMSO to prepare 100X dye mother liquor. On the other hand, if the dye is in liquid form, the manufacturer's recommended DMSO dissolved 100X mother liquor can be used. To prepare the dye for use, dilute the 100X mother liquor with the appropriate volume of the reaction solution to achieve a final dilution of 1:100. Additionally, DAPI can also be diluted accordingly with sterile water to prepare the working solution.
The secondary antibody provided in the kit is specifically designed for use with rabbit primary antibodies and is compatible with mouse tissue samples. Before beginning the experiment, it is important to verify whether the species of the primary antibody matches the secondary antibody. Please refer to the human sample (# ABS50012) for further information.
General Notes

1. This kit is only used for immunohistochemistry, not for other purposes.

2. This kit is for professional use only.

3. Appropriate protective measures should be taken to avoid contact with skin and eyes.

4. Do not use reagents that are past their expiry date because their activity may be reduced.

5. If the staining components of this kit are mixed with the products of other companies, abnormal conditions may occur during the dyeing process.

6 dewaxing is not complete, easy to affect the dyeing effect.

7. In order to prevent possible false negative and false positive results, it is necessary to have both positive and negative controls during the experiment.

8. All waste generated from the use of this kit should be treated in accordance with the Regulations on the Management of Medical Waste.

Overview
Storage Temp.
Fluorescent dye should be stored away from light, 2 ~ 8℃ storage, receipt of goods is valid for 12 months.
References
References
Diagnostic Immunohistochemistry (M). Beijing: Peking University Medical Press, 2008.9.2.【America】Ed Harlow, David Lane. Technical Guide for antibody (M). Beijing: Science Press, 2002:79-80,105.3.Stack, E. C., et al., vesicular ANATOMY and vesicular anatomy; imaging and quantitation: a review, with an assessment of Tyramide signal amplification, multispectral imaging and multiplex analysis. Methods, 2014, 70 (1) : 46-58.4. Qian Bangguo. Jiao Lei. Application of multilabel immunofluorescence staining and Doppler imaging in histological study. Chinese Journal of Histochemistry and Cytochemistry, 2017 (4): 373-382.


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