Cas9 Expressing Rat adrenal pheochromocytoma cells

Catalog Number: GEC0075

Price:

$3000

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Specifications

Product Information
Product Name	Cas9 Expressing Rat adrenal pheochromocytoma cells
Specification	1*10^6
System	endocrine system
Resistance	hygro
Cas9 expression detection	Provided
Cell name	PC-12-CAS9
Cell morphology	Epithelial like, adherent cells
passage ratio	1:3~1:5
Species expression gene	Rat
Expressed Gene	Cas9

Properties
Construction method	Viral method
Mycoplasma detection	negative
Storage and transportation	Dry ice transportation; Store in liquid nitrogen
Culture system	90% DMEM+10% FBS

Overview

PC-12-CAS9 is an advanced CRISPR/Cas9 gene-editing tool designed for precision genome modifications in a wide range of biological systems Utilizing the Cas9 nuclease which acts as molecular scissors PC-12-CAS9 enables targeted double-strand breaks in DNA at specific loci dictated by customizable guide RNAs This mechanism facilitates precise modifications such as gene knockouts insertions or replacements making it a vital tool for both functional genomics and therapeutic development

One of the key functions of PC-12-CAS9 is its ability to streamline the gene-editing process compared to traditional methods significantly reducing the time and resources needed for experiments Its high specificity minimizes off-target effects a critical consideration in research and therapeutic applications thus enhancing the reliability of experimental outcomes The product is optimized for various cell types including embryonic stem cells primary cells and cell lines providing a versatile platform for diverse research applications

The scientific importance of PC-12-CAS9 is underscored by its widespread applicability in research settings particularly in the fields of genetics developmental biology and regenerative medicine Furthermore it holds promise for use in clinical settings such as gene therapy cancer treatment and the modeling of genetic disorders paving the way for novel therapeutic approaches

Compared to alternative gene-editing solutions PC-12-CAS9 boasts a unique combination of efficiency specificity and user-friendly design making it an attractive option for researchers and clinicians alike Its comprehensive user manual and robust support from our technical team further enhance its accessibility for both novice and experienced users

Investing in PC-12-CAS9 not only empowers researchers to unlock complex biological questions but also offers clinicians innovative tools for advancing patient care Our company with its deep expertise in molecular biology and commitment to cutting-edge research solutions is proud to deliver this powerful tool to the scientific community fostering advancements in biology and medicine

Application

PC-12-CAS9 is primarily utilized in genetic research and therapeutic applications as a powerful tool for precise genome editing In research settings it is deployed for targeted modification of specific genes in various cell lines and animal models enabling scientists to investigate gene function disease mechanisms and pathways involved in neuronal development and differentiation For instance in neurobiological studies researchers use PC-12-CAS9 to knockout genes implicated in neurodegenerative diseases allowing them to assess phenotypic changes in neural phenotype or to explore potential therapeutic targets

Clinicians may also employ PC-12-CAS9 in cutting-edge gene therapy protocols aimed at treating genetic disorders by correcting mutations in patient-derived cells This innovative tool integrates seamlessly into workflows that utilize CRISPR-based techniques making it an ideal choice for multiplex gene editing experiments

The practical benefits of using PC-12-CAS9 include high specificity and efficiency in gene editing which helps reduce off-target effects and enhances the success rate of experiments Moreover PC-12-CAS9 is compatible with specialized protocols such as electroporation and viral delivery methods offering flexibility in implementation across diverse biological systems

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Please note that all services are for research use only. Not intended for any clinical use.

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