Human CD82/Kai-1 APC-conjugated Antibody Summary
Met1-Tyr267
Accession # AAH01821
Applications
Please Note: Optimal dilutions should be determined by each laboratory for each application. General Protocols are available in the Technical Information section on our website.
Scientific Data
Detection of CD82/Kai‑1 in Human Blood Lymphocytes by Flow Cytometry. Human peripheral blood lymphocytes were stained with Mouse Anti-Human CD82/Kai-1 APC-conjugated Monoclonal Antibody (Catalog # FAB4616A, filled histogram) or isotype control antibody (Catalog # IC002A, open histogram). View our protocol for Staining Membrane-associated Proteins.
Preparation and Storage
- 12 months from date of receipt, 2 to 8 °C as supplied.
Background: CD82/Kai-1
CD82, also known as KAI1, C33 and TSPAN27, is a widely expressed palmitoylated molecule in the tetraspanin superfamily. CD82 is synthesized as a 28 kDa core protein with mature molecular weights ranging up to 70 kDa due to variable glycosylation. CD82 functions as a suppressor of metastasis and is down‑regulated in many malignant tumors. It associates with IGSF8, DARC, the ganglioside GM2, and the HTLV-1 Gag protein. CD82 inhibits cell migration and metastasis by preventing integrin maturation and blocking integrin interactions with Met. Human CD82 shares 76% aa sequence identity with mouse and rat CD82.
Product Datasheets
Citations for Human CD82/Kai-1 APC-conjugated Antibody
R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.
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Defining the Skeletal Myogenic Lineage in Human Pluripotent Stem Cell-Derived Teratomas
Authors: MP Pappas, N Xie, JS Penaloza, SSK Chan
Cells, 2022-05-09;11(9):.
Species: Human
Sample Types: Whole Cells
Applications: Flow Cytometry -
Efficient Muscle Regeneration by Human PSC-Derived CD82+ ERBB3+ NGFR+ Skeletal Myogenic Progenitors
Authors: Ning Xie, Sabrina N. Chu, Cassandra B. Schultz, Sunny S. K. Chan
Cells
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