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UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
Conjugate:
unconjugated
Clone:
6D4, monoclonal
Application:
flow cytometry
immunohistochemistry
inhibition assay
immunohistochemistry
inhibition assay
Species reactivity:
human
Citations:
Technique(s):
flow cytometry: suitable
immunohistochemistry: suitable (paraffin)
inhibition assay: suitable
immunohistochemistry: suitable (paraffin)
inhibition assay: suitable
Uniprot accession no.:
产品名称
Anti-MIC-A MIC-B Antibody, clone 6D4, clone 6D4, from mouse
biological source
mouse
conjugate
unconjugated
antibody form
purified immunoglobulin
antibody product type
primary antibodies
clone
6D4, monoclonal
species reactivity
human
packaging
antibody small pack of 25 μg
technique(s)
flow cytometry: suitable
immunohistochemistry: suitable (paraffin)
inhibition assay: suitable
isotype
IgG2aκ
NCBI accession no.
UniProt accession no.
target post-translational modification
unmodified
Gene Information
human ... MICA(100507436)
Physical form
Protein G purified
Purified mouse monoclonal antibody IgG2a in PBS without azide.
Format: Purified
Analysis Note
Evaluated by Flow Cytometry in HeLa cells.
Flow Cytometry Analysis: 1 µg of this antibody detected MIC-A MIC-B in one million HeLa cells.
Flow Cytometry Analysis: 1 µg of this antibody detected MIC-A MIC-B in one million HeLa cells.
Application
Anti-MIC-A/MIC-B, Clone 6D4, Cat. No. MABF2160, is a mouse monoclonal antibody that detects MHC class I polypeptide-related sequence A/MHC class I polypeptide-related sequence B (MIC-A and MIC-B) and has been tested for use in Flow Cytometry, Immunohistochemistry (Paraffin), and Inhibition Activity/
Immunohistochemistry (Paraffin) Analysis: A representative lot detected MIC-A and MIC-B in Immunohistochemistry applications (Groh, V., et. al. (1999). Proc Natl Acad Sci U S A. 96(12):6879-84).
Flow Cytometry Analysis: A representative lot detected MIC-A and MIC-B in Flow Cytometry applications (Groh, V., et. al. (1999). Proc Natl Acad Sci U S A. 96(12):6879-84).
Inhibits Activity/Function Analysis: A representative lot inhibited cytotoxicity of ovary tumor-derived T cells against various cancer cell lines. (Groh, V., et. al. (1999). Proc Natl Acad Sci U S A. 96(12):6879-84).
Flow Cytometry Analysis: A representative lot detected MIC-A and MIC-B in Flow Cytometry applications (Groh, V., et. al. (1999). Proc Natl Acad Sci U S A. 96(12):6879-84).
Inhibits Activity/Function Analysis: A representative lot inhibited cytotoxicity of ovary tumor-derived T cells against various cancer cell lines. (Groh, V., et. al. (1999). Proc Natl Acad Sci U S A. 96(12):6879-84).
Research Category
Inflammation & Immunology
Inflammation & Immunology
Biochem/physiol Actions
Clone 6D4 specifically stains MIC-A and MIC-B in human cells.
Disclaimer
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
General description
42.91 and 42.64 kDa calculated, respectively for MIC-A and MIC-B.
MHC class I polypeptide-related sequence A/MHC class I polypeptide-related sequence B (UniProt: Q29983/Q29980; also known as MIC-A/MIC-B) is encoded by the MICA/MICB (also known as PERB11.1/PERB11.2) gene (Gene ID: 100507436/4277) in human. MIC-A and B are closely related single-pass type I membrane proteins that act as stress-induced self-antigen that are recognized by gamma-delta T cells and serve as ligands for the KLRK1/NKG2D receptor. They are recognized by cytotoxic gamma-delta T cells expressing the TCR variable region V delta1. Under normal conditions expression of MIC-A and B is restricted mainly to the intestinal epithelium. However, their expression has been reported in tumor cells. They are proteolytically cleaved and released from the cell surface of tumor cells which impairs KLRK1/NKG2D expression and T-cell activation. MIC-A and B can be induced by heat shock and by exposure to DNA damaging conditions. They are synthesized with a signal peptide (aa 1-23 and 1-22, respectively for MIC-A and MIC-B), which are cleaved off in the mature form. Their mature forms contain an extracellular domain (aa 24-304 and 23-309), a transmembrane domain (aa 308-328 and 310-330), and a cytoplasmic domain (aa 329-383 and 331-383), respectively. (Ref.: Groh, V., et al. (1999). Proc. Natl. Acad. Sci USA. 96 (12); 6879-6884).
Immunogen
C1R cells expressing MICA.
Other Notes
Concentration: Please refer to lot specific datasheet.
Preparation Note
Stable for 1 year at -20°C from date of receipt. Handling Recommendations: Upon receipt and prior to removing the cap, centrifuge the vial and gently mix the solution. Aliquot into microcentrifuge tubes and store at -20°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance.
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