
Five Color Multiplex Fluorescent Immunostaining Kit (Anti Rabbit)
Please note that the price mentioned is only for your reference. For detailed pricing information, we kindly request you to get in touch with our seller, Vecent. Thank you for your understanding.
Description
| SKU-Pack Size | Availability | Price |
| abs50029-20T | 1-2 weeks | $935.00 |
| abs50029-100T | n stock | $3557.00 |
Please note that the price mentioned is only for your reference. For detailed pricing information, we kindly request you to get in touch with our seller, Vecent. Thank you for your understanding.
| Description | |
| Description | The biological significance and clinical value of the tissue microenvironment can be attributed to its composition of intricate cells. These cells play a crucial role in determining the phenotype, state, abundance, and distribution within the tissue microenvironment. It can be shown in situ by antibody staining.Immunohistochemical staining is a widely used technique in the study of tissue morphology and protein expression within tissues. However, traditional IHC detection methods are limited in their ability to simultaneously display multiple indicators and effectively illustrate the cellular composition, condition, and intercellular relationships within complex tissue microenvironments. These aspects hold significant importance in the accurate diagnosis and treatment of various diseases. Hence, there is a need for improved techniques to overcome these limitations and provide a more comprehensive understanding of tissue characteristics and protein expression patterns. The principle behind the tyramide signal amplification technology is quite similar to the DAB color rendering method used in conventional immunohistochemistry. In this technique, a secondary antibody labeled with HRP is used. HRP then catalyzes the addition of a fluorescent substrate, which results in the production of an activated form of the substrate. This activated substrate has the ability to covalently bind with tyrosine on the antigen present in the sample, leading to stable covalent binding of the fluorescent substrate on the sample surface. Ultimately, this results in highly amplified signal amplification and increased sensitivity of the detection assay.Following the first incubation, which involved using a primary antibody and a luciferase substrate to bind non-covalently, hot repair was utilized to wash off any remaining antibodies. A subsequent round of incubation followed, which utilized another primary antibody and luciferase substrate, which allowed for multiple labeling to be achieved. This method ensured that a highly similar content was produced, while still preserving the original text information. It is essential to note that the generated content was produced using a language model, using a different technique than the ChapGPT-generated content. |
| Applications | This technique is primarily utilized in the immunohistochemical labeling of tissues from human or mouse specimens, as well as paraffin sections and TMA chips. To create a highly similar passage, we could rephrase the original statement as follows: The primary application of this method involves the use of immunohistochemistry to label human or mouse tissue samples, as well as paraffinized sections and tissue microarray chips. |
| Usage | To dilute fluorescent dye, first dissolve dry powder with 100ul of DMSO to create a 100X dye mother liquor. If the dye is already in liquid form, simply use the factory-provided DMSO-dissolved 100X mother liquor. Next, to prepare the dye working solution for use, dilute the signal amplification reaction solution at a 1:100 ratio. DAPI can be diluted with sterile water at a 1:100 ratio to create the working solution. When using a secondary antibody, ensure that it is compatible with the primary antibody species. In this particular kit, the anti-rabbit secondary antibody is suitable for mouse tissue samples. Before conducting the experiment, double-check to ensure that the species of the primary antibody matches. For reference, please see the human sample (# ABS50013). It is imperative to take note of the details in preparing and executing the experiment to guarantee successful outcomes. |
| 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.【美】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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