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> home > Products > Peptides > Biological Process > Cell Death > MICA Antibody (Center) Blocking Peptide
MICA Antibody (Center) Blocking PeptideSynthetic peptide
| Country | United States
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| Catalog # | Size | Availability | Price | |
| BP8626c | 0.1 mg 400 ul | In Stock | $ 45.00 | DISCONTINED INQUIRE CLICK INQUIRE Add to cart |
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MICA Antibody (Center) Blocking Peptide - Product info | |
| Primary Accession | Q29983 |
| Clone Names | 90713138 |
| Calculated MW | 42915 Da |
MICA Antibody (Center) Blocking Peptide - Additional info | |
| Gene ID 100507436 | |
| Target/Specificity The synthetic peptide sequence used to generate the antibody AP8626c was selected from the Center region of human MICA. A 10 to 100 fold molar excess to antibody is recommended. Precise conditions should be optimized for a particular assay. | |
| Format Synthetic peptide was lyophilized with 100% acetonitrile and is supplied as a powder. Reconstitute with 0.1 ml DI water for a final concentration of 1 mg/ml. | |
| Storage Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C. | |
| Precautions This product is for research use only. Not for use in diagnostic or therapeutic procedures. | |
MICA Antibody (Center) Blocking Peptide - Protein Information | |
| Name MICA | |
| Synonyms PERB11.1 | |
| Function Seems to have no role in antigen presentation. Acts as a stress-induced self-antigen that is recognized by gamma delta T- cells. Ligand for the KLRK1/NKG2D receptor. Binding to KLRK1 leads to cell lysis | |
| Cellular Location Cell membrane; Single-pass type I membrane protein. Cytoplasm. Note=Expressed on the cell surface in gastric epithelium, endothelial cells and fibroblasts and in the cytoplasm in keratinocytes and monocytes. Infection with human adenovirus 5 suppresses cell surface expression due to the adenoviral E3-19K protein which causes retention in the endoplasmic reticulum | |
| Tissue Location Widely expressed with the exception of the central nervous system where it is absent. Expressed predominantly in gastric epithelium and also in monocytes, keratinocytes, endothelial cells, fibroblasts and in the outer layer of Hassal's corpuscles within the medulla of normal thymus. In skin, expressed mainly in the keratin layers, basal cells, ducts and follicles Also expressed in many, but not all, epithelial tumors of lung, breast, kidney, ovary, prostate and colon. In thyomas, overexpressed in cortical and medullar epithelial cells. Tumors expressing MICA display increased levels of gamma delta T-cells | |
MICA Antibody (Center) Blocking Peptide - Related products
MICA Antibody (Center) Blocking Peptide - Research Areas
PeptidesBiological ProcessCell DeathT Cell ActivationCellular ProcessPositive Regulation Of Biological ProcessRegulation Of Response To StimulusRegulation Of Response To StressRegulation Of Immune System ProcessResponse To StressDeathCellular Response To StimulusCellular Response To StressRegulation Of Immune ResponsePositive Regulation Of Response To StimulusMulti-organism ProcessBiological RegulationResponse To Abiotic StimulusRegulation Of Defense ResponseImmune Effector ProcessRegulation Of Biological ProcessCell ActivationPositive Regulation Of Immune ResponseResponse To StimulusActivation Of Immune ResponsePositive Regulation Of Immune System ProcessLymphocyte ActivationLeukocyte ActivationImmune System ProcessRegulation Of Innate Immune ResponseResponse To Temperature StimulusPositive Regulation Of Defense ResponsePositive Regulation Of Innate Immune ResponseImmune Response-activating Signal TransductionResponse To Biotic Stimulus
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Provided below are standard protocols that you may find useful for product applications.
BACKGROUND
MICA is the higly polymorphic MHC (HLA) class I chain-related gene A. The protein product is expressed on the cell surface, although unlike canonical class I molecules does not seem to associate with beta-2-microglobulin. It is thought that MICA functions as a stress-induced antigen that is broadly recognized by intestinal epithelial gamma delta T cells.
REFERENCES
Bahram,S., et.al., Proc. Natl. Acad. Sci. U.S.A. 91 (14), 6259-6263 (1994)Klein,J.et.al., Proc. Natl. Acad. Sci. U.S.A. 91 (14), 6251-6252 (1994)Parham,P., et.al., J. Immunol. 142 (11), 3937-3950 (1989)
