Rabbit Polyclonal SLAMF7/CS1 antibody. Suitable for IHC-P and reacts with Mouse, Human samples. Cited in 4 publications. Immunogen corresponding to Synthetic Peptide within Human SLAMF7 aa 50-150 conjugated to Keyhole Limpet Haemocyanin.
View Alternative Names
CD319, CS1, UNQ576/PRO1138, SLAMF7, SLAM family member 7, CD2 subset 1, CD2-like receptor-activating cytotoxic cells, Membrane protein FOAP-12, Novel Ly9, Protein 19A, CRACC
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SLAMF7/CS1 antibody (AB202840)
Immunohistochemical analysis of Formalin fixed paraffin-embedded Mouse intestine tissue labeling SLAMF7/CS1 with ab202840 at 1/200 dilution.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SLAMF7/CS1 antibody (AB202840)
Immunohistochemical analysis of Formalin fixed paraffin-embedded Mouse stomach tissue labeling SLAMF7/CS1 with ab202840 at 1/200 dilution.
Reactivity data
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Supplementary information
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Biological function summary
SLAMF7/CS1 modulates immune functions by engaging in interactions with other cell surface receptors. It often operates in the context of hematopoietic cells integrating signals that influence cell proliferation differentiation and survival. It does not require an associated adaptor molecule like most of the SLAM family members as it signals through its ability to recruit EAT-2. The CS1 protein modulates pathways related to immune cell activation and control making it an important player in the regulation of immune responses.
Pathways
CS1 participates prominently in immune signaling pathways where it interacts with proteins such as SAP and EAT-2. It is particularly involved in the immunoregulatory interactions contributing to NK cell-mediated cytotoxicity and modulation of T-cell responses. These interactions illustrate CS1's role in the modulation of immune responses positioning it within the broader network of immune signaling pathways important for maintaining immune homeostasis and defense mechanisms.
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Target data
Publications (4)
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Nature nanotechnology 17:1332-1341 PubMed36357792
2022
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Oncology letters 24:433 PubMed36311690
2022
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Cancers 14: PubMed36230572
2022
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Scientific reports 7:42646 PubMed28211524
2017
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Product promise
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