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Human SIGLEC10 Stable Cell Line - CHO-K1

Human SIGLEC10 Stable Cell Line - CHO-K1

Cat.No. :  CSC-RO0473 Host Cell:  CHO-K1

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Cell Line Information

Cell Culture Information

Safety and Packaging

Cat. No. CSC-RO0473
Description This cell line is derived from CHO-K1 and is engineered to stably overexpress Human SIGLEC10.
Gene SIGLEC10
Gene Species Homo sapiens (Human)
Host Cell CHO-K1
Host Cell Species Cricetulus griseus (Chinese hamster)
Stability Validated for at least 10 passages
Application

1. Studying the interactions between immune cells and cancer cells

2. Studying the mechanisms of resistance to immune checkpoint blockade

3. High-throughput screening

4. Drug target validation

Quality Control Negative for bacteria, yeast, fungi and mycoplasma.
Shipping Dry ice
Storage Liquid nitrogen
Revival Rapidly thaw cells in a 37°C water bath. Transfer contents into a tube containing pre-warmed media. Centrifuge cells and seed into a 25 cm2 flask containing pre-warmed media.
Mycoplasma Negative
Format One frozen vial containing millions of cells
Storage Liquid nitrogen
Safety Considerations

The following safety precautions should be observed.

1. Use pipette aids to prevent ingestion and keep aerosols down to a minimum.

2. No eating, drinking or smoking while handling the stable line.

3. Wash hands after handling the stable line and before leaving the lab.

4. Decontaminate work surface with disinfectant or 70% ethanol before and after working with stable cells.

5. All waste should be considered hazardous.

6. Dispose of all liquid waste after each experiment and treat with bleach.

Ship Dry ice
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Background

Case Study

Applications

Publications

Q & A

Customer Reviews

Stable cell line for humans SIGLEC10 Sialic Acid Binding Ig Like Lectin 10 (SIGLEC10), a member of the immunoglobulin superfamily expressed on the cell surface, is expressed in the CHO-K1 cell line. Mostly present on innate immune system cells, SIGLECs usually have one or more cytoplasmic immune receptor tyrosine-based inhibitory motifs (ITIMs). Sialic-acid dependent adherence to cells is mediated by SIGLEC10, a potential adhesion molecule that prefers alpha-2,3- or alpha-2,6-linked sialic acid and is encoded by the SIGLEC10 gene on chromosome 19q13.41. By attracting cytoplasmic phosphatases via their SH2 domains and preventing signal transmission, it might function as an inhibitory receptor in response to ligand-induced tyrosine phosphorylation. In conjunction with CD24, SIGLEC10 has a role in the negative regulation of B-cell antigen receptor signaling and has the ability to specifically inhibit the immunological response to danger-associated molecular patterns (DAMPs). Chinese hamster ovary cells are the source of CHO-K1 cells, which are widely employed in biotechnology and pharmaceutical research. These are adherent cells that proliferate as monolayers in culture or in suspension. Because CHO-K1 cells may be genetically modified and have their proteins expressed, they can be used to create stable cell lines that express certain genes of interest.

SIGLEC10's critical function in gastric cancer (GC) is highlighted by the researchers through an examination of its effects on CD8 T cells that have invaded tumors. Through in vitro tests, they demonstrate that SIGLEC10, which is expressed on CD68 macrophages, blocks the Akt/P38/Erk signaling pathway, which in turn reduces CD8 T cell activity and proliferation. Furthermore, SIGLEC10 inhibition improves CD8 T cell effector activity in both in vivo and ex vivo settings. Significantly, a poor prognosis for GC is linked to SIGLEC10 macrophages. These results highlight SIGLEC10's role as a direct inhibitor of T cell function, pointing to possible uses for it as an immunotherapeutic target and GC prognostic marker.

Figure 1 illustrates that SIGLEC10 macrophages in gastric cancer impede the function of infiltrating CD8 T cells, as evidenced by FACS analysis showing correlations between SIGLEC10 macrophage levels and the expression of CD8 T cell functional markers as well as exhausted markers. (doi: 10.1007/s00262-023-03488-2)Figure 1. Using a pHR lentiviral vector, the researchers cloned SIGLEC10 to produce overexpressing cell lines. Lentivoresis was observed when PHR-SIGLEC10-SFFV-IRES-EGFP was co-transfected into HEK293T cells along with additional plasmids. After infecting THP-1 cells with these, the cells were centrifuged and incubated to aid in the transfer of genes. The consequences of SIGLEC10 overexpression can be studied thanks to this technique. (Guo Y, et al., 2023)

1. Research on Immunotherapy: Make use of the stable cell line SIGLEC10 to examine immune response modification and possible uses in immunotherapy. 2. Cancer Research: Examine SIGLEC10's function in suppressing B-cell antigen receptor signaling in order to create cancer therapies. 3. Drug Development: To help with drug discovery, use CHO-K1 cells that express SIGLEC10 to screen for substances that alter immune responses. 4. Studies on Inflammatory Diseases: Examine SIGLEC10's capacity to suppress DAMP-induced immune reactions, which is important for comprehending and managing inflammatory illnesses. 5. Cell Adhesion Mechanisms: To understand cell adhesion mechanisms in health and illness, investigate SIGLEC10-mediated sialic-acid dependent adherence to cells.
Customer Q&As
How stable is this human SIGLEC10 stable cell line? Is there relevant quality control data?

A: Our human SIGLEC10 stable cell line has undergone rigorous stability testing and maintains stable expression levels over multiple passages. We regularly validate cell lines and record cell line stability data. Customers can request this data from us to understand the stability performance of our products.

How functional is this stable cell line when studying SIGLEC10-mediated immune regulatory mechanisms? Is relevant functional verification data provided?

A: Our human SIGLEC10 stable cell line is fully functional and widely used in research related to immune regulation. We provide detailed functional verification data, including cell signaling pathway analysis, apoptosis experiments, etc. Customers can refer to these data to evaluate the performance of our products.

Is this human SIGLEC10 stable cell line feasible for in vivo experiments?

A: Although our human SIGLEC10 stable cell line is mainly used for in vitro research, we can also provide relevant in vivo research data support, proving the application potential of our products in in vivo models. Customers can refer to this data to understand the performance and range of applications of our products in in vivo studies.

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Customer Reviews
Stability

In terms of gene expression, the expression of SIGLEC10 is very stable, which is very important for studying the function and signaling mechanism of cell surface glycoproteins. The morphology of the cells is good and there are no abnormal changes, and the accuracy of the experimental data is guaranteed. CHO-K1 cells are used for their excellent protein expression capabilities and ease of operation.

Canada

10/10/2020

Reliability

The gene expression of SIGLEC10 is stable, ensuring the reliability of research data. The platform provides detailed instructions and technical support, and the entire user experience is very professional and satisfying. Whether it is product quality or service level, this product is highly recommended.

United States

12/02/2020

High quality

While conducting research using the Human SIGLEC10 Stable Cell Line - CHO-K1, I found that this cell line is ideal for studying glycoprotein function in the innate immune system. The cells grew rapidly in the culture medium and maintained good shape and vitality. Overall, this cell line performs well in research applications and is an ideal tool for further research.

French

04/21/2021

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