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SSR2 Knockout Cell Lines

Gene: SSR2

Official Full Name: signal sequence receptor subunit 2provided by HGNC

Gene Summary: The signal sequence receptor (SSR) is a glycosylated endoplasmic reticulum (ER) membrane receptor associated with protein translocation across the ER membrane. The SSR consists of 2 subunits, a 34-kD glycoprotein (alpha-SSR or SSR1) and a 22-kD glycoprotein (beta-SSR or SSR2). The human beta-signal sequence receptor gene (SSR2) maps to chromosome bands 1q21-q23. [provided by RefSeq, Jul 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO35231 SSR2 Knockout cell line (HeLa) Human SSR2 1:3~1:6 Negative Online Inquiry
KO35232 SSR2 Knockout cell line (HCT 116) Human SSR2 1:2~1:4 Negative Online Inquiry
KO35233 SSR2 Knockout cell line (HEK293) Human SSR2 1:3~1:6 Negative Online Inquiry
KO35234 SSR2 Knockout cell line (A549) Human SSR2 1:3~1:4 Negative Online Inquiry

Background

SSR2 Gene Knockout Cell Lines are specially engineered cellular models designed to facilitate research into the functional roles of the SSR2 gene. These cell lines have undergone targeted genetic modification to create knockout organisms, meaning that the SSR2 gene has been completely disrupted, enabling scientists to study the consequential biological changes that occur in its absence. By generating these knockout models, researchers can dissect the pathways and mechanisms influenced by SSR2, thus contributing to a greater understanding of its role in various physiological and pathological contexts.

The primary function of SSR2 knockout cell lines is to provide a robust platform for investigating gene function, protein interactions, and cellular responses. Utilizing CRISPR/Cas9 or similar genome-editing technologies, these cell lines allow for precise alterations in the gene of interest, enabling scientists to observe phenotypic variations, signaling cascade modifications, and potential compensatory mechanisms that emerge upon gene disruption. Furthermore, such models are invaluable in elucidating disease mechanisms, particularly in cancer and metabolic disorders where SSR2 may play a pivotal role.

The scientific importance of SSR2 Gene Knockout Cell Lines lies in their wide-ranging applications, from basic research endeavors to translational studies in clinical settings. These cell lines serve as critical tools in drug discovery, toxicology assessment, and therapeutic intervention strategies, ultimately aiding in the development of targeted therapies that improve patient outcomes.

Compared to alternative knockout models or standard cell lines, SSR2 Gene Knockout Cell Lines offer enhanced specificity and reliability. They provide a complete absence of the SSR2 gene, allowing researchers to confidently attribute observed effects directly to the loss of gene function, thereby reducing background noise often encountered with partial knockdowns or overexpression studies.

For researchers and clinicians alike, the value of SSR2 Gene Knockout Cell Lines resides in their capability to unlock new insights into gene functions and interactions that could lead to significant advancements in therapeutic development. By utilizing these specialized models, users can substantially expedite their research timeline while enhancing the precision of their experimental results.

Our company prides itself on its expertise in providing high-quality biological products, leveraging advanced genetic engineering techniques to support innovative research efforts. Our SSR2 Gene Knockout Cell Lines represent a commitment to facilitating groundbreaking discoveries in molecular biology and medicine.

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

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