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HOME > Product search results > Code No. D263-3 Anti-CD63 (LAMP-3) (Mouse) mAb

Code No. D263-3

Anti-CD63 (LAMP-3) (Mouse) mAb

Availability (in Japan)

10 or more

(In Japan at 00:05,
Nov 20, 2018 in JST)

Size

100 µg/100 µL

Data
  • Flow Cytometry

Clonality Monoclonal Clone R5G2
Isotype (Immunized Animal) Rat IgG2b
Applications
IC*
reported.  (PMID: 20236428
FCM
10 µg/mL (final concentration)  
WB
2-10 µg/mL  
Other(Immuno-EM)
reported.  (PMID: 28956068 / 29669945
Immunogen (Antigen) Mouse bone marrow stroma cell line ST2
Reactivity [Gene ID]

Mouse[12512]

Storage buffer 1 mg/mL in PBS/50% glycerol, pH 7.2
Storage temp. -20°C Conjugate Unlabeled Manufacturer MBL
Alternative names ME491, C75951, Tspan30
Background CD63 is not only expressed on activated platelets, but also activated monocytes and macrophages, and is weakly expressed on granulocytes, T cell and B cells. It is located on the basophilic granule membranes and translocated to cell surface upon various stimuli. The membrane of lytic granules in CTLs contains CD63/LAMP-3 and other lysosomal-associated glycoproteins (LAMPs) such as CD107a/LAMP-1 and CD107b/LAMP-2. LAMPs have been observed on the cell surface as a result of degranulation. CD63 belongs to a member of the tetraspanin transmembrane-protein (TM4) superfamily, which includes CD9, CD37, CD53, CD81, CD82, CD151 and CD231. Several members of this family form noncovalent associations with integrins, particularly b1 integrins (CD29), and modulate cellular adhesion properties. CD63 has a tyrosine-based internalization motif in the cytoplasmic C-terminal tail and interacts with adaptor protein complexes such as AP-2 and AP-3. Because AP-2 and AP-3 are involved in facilitating the clathrin-mediated endocytosis, CD63 could be directly involved in the internalization of its membrane protein partners.
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Citations

Western Blotting

  1. Seto S et al. Differential recruitment of CD63 and Rab7-interacting-lysosomal-protein to phagosomes containing Mycobacterium tuberculosis in macrophages. Microbiol Immunol. 54,170-4 (2010)(PMID:20236428)
  2. Ushio H et al. Crucial role for autophagy in degranulation of mast cells. J Allergy Clin Immunol. 127, 1267-76 (2011)(PMID:21333342)
  3. Bobrie A et al. Diverse subpopulations of vesicles secreted by different intracellular mechanisms are present in exosome preparations obtained by differential ultracentrifugation. J Extracell Vesicles. 1, 18397 (2012)(PMID:24009879)
  4. Padro CJ et al. Adrenergic regulation of IgE involves modulation of CD23 and ADAM10 expression on exosomes. J Immunol. 191, 5383-97 (2013)(PMID:24140643)
  5. Zonneveld MI et al. Recovery of extracellular vesicles from human breast milk is influenced by sample collection and vesicle isolation procedures. J Extracell Vesicles. 3, 24215 (2014)(PMID:25206958)
  6. Groot Kormelink T et al. Prerequisites for the analysis and sorting of extracellular vesicle subpopulations by high-resolution flow cytometry. Cytometry A. 89, 135-47 (2016)(PMID:25688721)
  7. Kowal J et al. Proteomic comparison defines novel markers to characterize heterogeneous populations of extracellular vesicle subtypes. PNAS. 113, E968-77 (2016)(PMID:26858453)
  8. Groot Kormelink T et al. Mast Cell Degranulation Is Accompanied by the Release of a Selective Subset of Extracellular Vesicles That Contain Mast Cell-Specific Proteases. J Immunol. 197, 3382-3392 (2016)(PMID:27619994)
  9. Nager AR et al. An Actin Network Dispatches Ciliary GPCRs into Extracellular Vesicles to Modulate Signaling. Cell 168, 252-263.e14 (2017)(PMID:28017328)
  10. Nishida-Aoki N et al. Disruption of Circulating Extracellular Vesicles as a Novel Therapeutic Strategy against Cancer Metastasis. Mol Ther. 25, 181-191 (2017)(PMID:28129113)
  11. Durcin M et al. Characterisation of adipocyte-derived extracellular vesicle subtypes identifies distinct protein and lipid signatures for large and small extracellular vesicles. J Extracell Vesicles. 6,1305677 (2017)(PMID:28473884)
  12. Iraci N et al. Extracellular vesicles are independent metabolic units with asparaginase activity. Nat Chem Biol. 13, 951-955 (2017)(PMID:28671681)
  13. Laulagnier K et al. Amyloid precursor protein products concentrate in a subset of exosomes specifically endocytosed by neurons. Cell Mol Life Sci. 75, 757-773 (2018)(PMID:28956068)
  14. Krause M et al. Exosomes as secondary inductive signals involved in kidney organogenesis. J Extracell Vesicles. 7, 1422675 (2018)(PMID:29410779)
  15. Obata Y et al. Adiponectin/T-cadherin system enhances exosome biogenesis and decreases cellular ceramides by exosomal release. JCI Insight 3, e99680 (2018)(PMID:29669945)

Flow Cytometry

  1. Kunert S et al. The microtubule modulator RanBP10 plays a critical role in regulation of platelet discoid shape and degranulation. Blood 114, 5532-40 (2009)(PMID:19801445)
  2. Ushio H et al. Crucial role for autophagy in degranulation of mast cells. J Allergy Clin Immunol. 127, 1267-76 (2011)(PMID:21333342)
  3. Verjan Garcia N et al. SIRPα/CD172a regulates eosinophil homeostasis. J Immunol. 187, 2268-77 (2011)(PMID:21775684)
  4. Brochetta C et al. Munc18-2 and syntaxin 3 control distinct essential steps in mast cell degranulation. J Immunol. 192, 41-51 (2014)(PMID:24323579)

Immunocytochemistry

  1. Seto S et al. Differential recruitment of CD63 and Rab7-interacting-lysosomal-protein to phagosomes containing Mycobacterium tuberculosis in macrophages. Microbiol Immunol. 54,170-4 (2010)(PMID:20236428)
  2. Ushio H et al. Crucial role for autophagy in degranulation of mast cells. J Allergy Clin Immunol. 127, 1267-76 (2011)(PMID:21333342)
  3. Päll T et al. Soluble CD44 interacts with intermediate filament protein vimentin on endothelial cell surface. PLoS One 6, e29305 (2011)(PMID:22216242)
  4. Lopes da Silva M et al. The host endocytic pathway is essential for Plasmodium berghei late liver stage development. Traffic. 13, 1351-63 (2012)(PMID:22780869)
  5. Bobrie A et al. Diverse subpopulations of vesicles secreted by different intracellular mechanisms are present in exosome preparations obtained by differential ultracentrifugation. J Extracell Vesicles. 1, 18397 (2012)(PMID:24009879)
  6. Krause M et al. Exosomes as secondary inductive signals involved in kidney organogenesis. J Extracell Vesicles. 7, 1422675 (2018) (PMID:29410779)
  7. Obata Y et al. Adiponectin/T-cadherin system enhances exosome biogenesis and decreases cellular ceramides by exosomal release. JCI Insight 3, e99680 (2018)(PMID:29669945)

Other(Immuno-EM)

  1. Laulagnier K et al. Amyloid precursor protein products concentrate in a subset of exosomes specifically endocytosed by neurons. Cell Mol Life Sci. 75, 757-773 (2018)(PMID:28956068)
  2. Obata Y et al. Adiponectin/T-cadherin system enhances exosome biogenesis and decreases cellular ceramides by exosomal release. JCI Insight 3, e99680 (2018)(PMID:29669945)
Product category
Research area
Immunology
Cancer
Cell surface antigens
Exosomes
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  • The availability is based on the information in Japan at 00:05, Nov 20, 2018 in JST.
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  • Please note that products cannot be ordered from this website. To purchase the items listed in this website, please contact us or local distributers.
  • Abbreviations for applications:
    WB: Western Blotting, IH: Immunohistochemistry, IC: Immunocytochemistry, IP: Immunoprecipitation
    FCM: Flow Cytometry, NT: Neutralization, IF: Immunofluorescence, RIP: RNP Immunoprecipitation
    ChIP: Chromatin Immunoprecipitation, CoIP: Co-Immunoprecipitation
  • For applications and reactivity:
    *: The use is reported in a research article (Not tested by MBL). Please check the data sheet for detailed information.
    **: The use is reported from the licenser (Under evaluation or not tested by MBL).
  • For storage temparature: RT: room temparature
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