HAVCR1
Purified Mouse Monoclonal Antibody
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Application
| WB, IHC, ICC, E |
---|---|
Primary Accession | Q96D42 |
Reactivity | Human |
Host | Mouse |
Clonality | Monoclonal |
Clone Names | 3A12E10 |
Isotype | Mouse IgG1 |
Calculated MW | 38.7kDa |
Immunogen | Purified recombinant fragment of human HAVCR1 (AA: 70-290) expressed in E. Coli. |
Formulation | Purified antibody in PBS with 0.05% sodium azide |
Gene ID | 26762 |
---|---|
Other Names | TIM; KIM1; TIM1; CD365; HAVCR; KIM-1; TIM-1; TIMD1; TIMD-1; HAVCR-1 |
Dilution | E~~ 1/10000 WB~~ 1/500 - 1/2000 |
Storage | Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles. |
Precautions | HAVCR1 is for research use only and not for use in diagnostic or therapeutic procedures. |
Name | HAVCR1 |
---|---|
Synonyms | KIM1, TIM1, TIMD1 |
Function | Phosphatidylserine receptor that plays an important functional role in regulatory B-cells homeostasis including generation, expansion and suppressor functions (By similarity). As P- selectin/SELPLG ligand, plays a specialized role in activated but not naive T-cell trafficking during inflammatory responses (PubMed:24703780). Controls thereby T-cell accumulation in the inflamed central nervous system (CNS) and the induction of autoimmune disease (PubMed:24703780). Regulates also expression of various anti- inflammatory cytokines and co-inhibitory ligands including IL10 (By similarity). Acts as a regulator of T-cell proliferation (By similarity). May play a role in kidney injury and repair (PubMed:17471468). |
Cellular Location | Cell membrane; Single-pass type I membrane protein |
Tissue Location | Widely expressed, with highest levels in kidney and testis. Expressed by activated CD4+ T-cells during the development of helper T-cells responses. |
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Provided below are standard protocols that you may find useful for product applications.
References
1.Biomed Res Int. 2015;2015:854070. 2.Pediatr Res. 2015 Oct;78(4):430-5.
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