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JAM-A / F11R / CD321 Antikörper ( FITC )

Sino Biological Inc. liefert JAM-A / F11R / CD321 Antikörper ( FITC ) mit höherer Qualität und günstiger Kosten im Vergleich mit anderen globalen Lieferanten.

Weitere Informationen über JAM-A / F11R / CD321 Antikörper ( FITC ) lesen Sie bitte: http://www.sinobiological.com/JAM-A-F11R-CD321-Antibody-g-10066.html

Produkt-Information von JAM-A / F11R / CD321 Antikörper

Immunogen

Recombinant Human JAM-A / F11R / CD321 protein (Catalog#10198-H08H)

Reagents FITC-conjugated mouse monoclonal antibody

Clone ID

04

Ig Type

 

Concentration

5 μl/Test, 0.2 mg/ml

Formulation Aqueous solution containing 0.5% BSA and 0.1% sodium azide
Preparation

This antibody was produced from a hybridoma resulting from the fusion of a mouse myeloma with B cells obtained from a mouse immunized with purified, recombinant Human JAM-A / F11R / CD321 (rh JAM-A / F11R / CD321; Catalog#10198-H08H; NP_058642.1; Met 1-Ala 242) and conjugated with FITC under optimum conditions, the unreacted FITC was removed.

Usage Guide von JAM-A / F11R / CD321 Antikörper

Specificity

Human JAM-A / F11R / CD321

Flow Cytometry
JAM-A / F11R / CD321 Flow Cytometry

Profile of anti-JAM-A (CD321) reactivity on SKBR3 cells analyzed by flow cytometry.

Flow cytometry was performed on a BD FACSCalibur flow cytometry system

Please refer to www.sinobiological.com/Flow-Cytometry-FACS-Protocols-a-750.html for technical protocols.

Storage This antibody is stable for 12 months from date of receipt when stored at 2℃-8℃. Protected from prolonged exposure to light. Do not freeze !
Sodium azide is toxic to cells and should be disposed of properly. Flush with large volumes of water during disposal.

Verwandte Produkte & Themen von JAM-A / F11R / CD321 Antikörper

Related Areas:

Cancer>>Angiogenesis>>Adhesion Molecules in Angiogenesis>>JAM-A/F11R/CD321

Immunology>>Adhesion Molecule>> Cell Adhesion Molecule (IgSF CAM) >>JAM-A/F11R/CD321

Immunology>>Cluster of Differentiation>>Other>>JAM-A/F11R/CD321

Proteins:
Molecule Species Description //For Detailed Info. and Price------CLICK! Cat. No
JAM-A/F11R/CD321 Human JAM-A/F11R/Fc Protein, Recombinant 10198-H02H
JAM-A/F11R/CD321 Human JAM-A/F11R Protein, Recombinant 10198-H08H
JAM-A/F11R Mouse JAM-A/F11R/Fc Protein, Recombinant 50463-M02H
JAM-A/F11R Rat F11R / JAM-A / JAM-1 Protein, Recombinant 80240-R02H
JAM-A/F11R Rat F11R / JAM-A / JAM-1 Protein, Recombinant 80240-R08H
Antibodies:
Molecule Application Description //For Detailed Info. and Price------CLICK! Cat. No
Human
JAM-A/F11R/CD321
ELISA Mouse Monoclonal Antibody 10198-MM02
Human
JAM-A/F11R/CD321
WB Mouse Monoclonal Antibody 10198-MM03
Human
JAM-A/F11R/CD321
FCM JAM-A / F11R / CD321 Antibody ( FITC ) 10198-MM04-F
Human
JAM-A/F11R/CD321
FCM JAM-A / F11R / CD321 Antibody ( PE ) 10198-MM04-P
Human
JAM-A/F11R/CD321
ELISA Rabbit Polyclonal Antibody 10198-RP01
Human
JAM-A/F11R/CD321
WB, ELISA Rabbit Polyclonal Antibody (Antigen Affinity Purified) 10198-RP04

Hintergrund von JAM-A / F11R / CD321 Antikörper

As a type Itransmembrane receptor belonging to the immunoglobulin superfamily, the human JAM-A, also known as platelet adhesion molecule 1 (PAM-1) and platelet F11 receptor, is the firstly identified member of the Junctional Adhesion Molecule (JAM) family comprising at least three members. JAM-A is specifically localized in tight junctions of epithelial and endothelial cells and is involved in the regulation of junctional integrity and permeability by serving as a physical barrier in a homophilic manner. JAM-A is also expressed on the surface of hematopoeitic cells, such as platelets and leukocytes, and acts as a ligand for integrin LFA-1 or a platelet receptor, consequently plays key roles in a variety of cellular processes, including platelet aggregation, leukocyte transmigration, and angiogenesis. In addition, JAM-A has also been implicated in the attachment of reovirus that causes diarrhea in human.

References

  1. Williams, L.A. et al., 1999, Mol.Immunol. 36:1175-1188.
  2. Sobocka, M.B. et al., 2000, Blood. 95: 2600-2609.
  3. Babinska, A. et al., 2002, Thromb. Haemost. 88: 843-850.
  4. Ostermann, G., et al., 2002, Nat. Immunol. 3: 151-158.
  5. Kenneth J. et al., 2005, J. Biol. Chem. 280: 11665-11674.
  6. Bazzoni G. et al., 2003, Curr.Opin.Cell.Biol. 15: 525-530.
  7. Barton, E. S. et al., 2001, Cell. 104: 441-451.

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