biological source
mouse
conjugate
unconjugated
antibody form
purified antibody
antibody product type
primary antibodies
clone
CSTEM27, monoclonal
mol wt
calculated mol wt 32.58 kDa
observed mol wt ~32 kDa
purified by
using protein G
species reactivity
human
packaging
antibody small pack of 100 μg
technique(s)
flow cytometry: suitable
western blot: suitable
isotype
IgG2aκ
epitope sequence
Extracellular domain
Protein ID accession no.
UniProt accession no.
shipped in
2-8°C
target post-translational modification
unmodified
Quality Level
Gene Information
human ... F11R(50848)
Application
Quality Control Testing
Evaluated by Western Blotting with recombinant Human JAM-A/F11R protein.
Western Blotting Analysis: A 1:1,000 dilution of this antibody detected recombinant Human JAM-A/F11R protein.
Tested Applications
Flow Cytometry Analysis: A representative lot detected JAM-A/F11R in Flow Cytometry application (Liu, X., et al. (2017). Nat Methods. 14(11); 1055-1062; O Brien, C.M., et al. (2017). Stem Cells. 35(3); 626-640; Liu, X., et al. (2020). Nature. 586(7827); 101-107).
ELISA Analysis: A representative lot detected JAM-A/F11R in ELISA application (O Brien, C.M., et al. (2017). Stem Cells. 35(3); 626-640).
Immunocytochemistry Analysis: A representative lot detected JAM-A/F11R in Immunocytochemistry application (O Brien, C.M., et al. (2017). Stem Cells. 35(3); 626-640).
Note: Actual optimal working dilutions must be determined by end user as specimens, and experimental conditions may vary with the end user
Evaluated by Western Blotting with recombinant Human JAM-A/F11R protein.
Western Blotting Analysis: A 1:1,000 dilution of this antibody detected recombinant Human JAM-A/F11R protein.
Tested Applications
Flow Cytometry Analysis: A representative lot detected JAM-A/F11R in Flow Cytometry application (Liu, X., et al. (2017). Nat Methods. 14(11); 1055-1062; O Brien, C.M., et al. (2017). Stem Cells. 35(3); 626-640; Liu, X., et al. (2020). Nature. 586(7827); 101-107).
ELISA Analysis: A representative lot detected JAM-A/F11R in ELISA application (O Brien, C.M., et al. (2017). Stem Cells. 35(3); 626-640).
Immunocytochemistry Analysis: A representative lot detected JAM-A/F11R in Immunocytochemistry application (O Brien, C.M., et al. (2017). Stem Cells. 35(3); 626-640).
Note: Actual optimal working dilutions must be determined by end user as specimens, and experimental conditions may vary with the end user
Anti-JAM-A/F11R, clone CSTEM27, Cat. No. MABT1541, is a mouse monoclonal antibody that detects Junctional adhesion molecule A (JAM-A/FR11) and is tested for use in ELISA, Flow Cytometry, Immunocytochemistry, and Western Blotting.
Biochem/physiol Actions
Clone CSTEM27 is a mouse monoclonal antibody that detects Junctional adhesion molecule A (JAM-A/FR11). It targets an epitope within the extracellular domain.
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
Junctional adhesion molecule A (UniProt: Q9Y624; also known as JAM-A, Junctional adhesion molecule 1, JAM-1, Platelet F11 receptor, Platelet adhesion molecule 1, PAM-1, CD321) is encoded by the F11R (also known as JAM1, JCAM) gene (Gene ID: 50848) in human. JAM-A/F11R is a single-pass type I membrane protein that is localized at tight junctions of both epithelial and endothelial cells. It is also expressed in circulating platelets and leukocytes. It is synthesized with a signal peptide (aa 1-27), which is subsequently cleaved off to produce the mature form that contains an extracellular domain (aa 28-238), a transmembrane domain (aa 239-259), and a cytoplasmic domain (aa 260-299). The extracellular domain contains a membrane distal VH-type Ig-like domain (D1; aa 28-125) and a membrane proximal C2-type Ig-like domain (D2; aa 135-228) that contains a single glycosylation site (Asn 185). The cytoplasmic domain includes two phosphorylation sites (Tyr 280 and Ser 284) and also has a type II PDZ domain-binding motif (aa 297-299). JAM-A/F11R plays a role in epithelial tight junction formation and also regulates monocyte transmigration involved in integrity of epithelial barrier. It participates in the regulation of various biological processes, including paracellular permeability, tight junction formation and maintenance, leukocyte trans-endothelial migration, epithelial-to-mesenchymal transition (EMT), angiogenesis, reovirus binding, and platelet activation. Its dysregulation may contribute to pathological consequences, such as cardiovascular diseases, inflammatory bowel disease, neurological disorders, and various cancer types. In cancer cells, it is not only associated with regulation of cell migration, but it also affects apoptosis, EMT, cancer stem cell maintenance, and cell proliferation. Down-regulation of JAM-A/F11R results in elevated cell migration, invasion, and metastasis in various breast cancer cell lines. Its higher levels have been linked to reduced cell migration ability of cancer cells. (Ref.: Czubak-Prowizor, K., et al. (2022). Mol. Cell. Biochem. 477(1); 79-98; Liu, X., et al. (2020). Nature. 586(7827); 101-107).
Immunogen
His-tagged recombinant fragment corresponding to the extracellular domain of human Junctional adhesion molecule A (JAM-A/F11R).
Other Notes
Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.
Physical form
Purified mouse monoclonal antibody IgG2a in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.
Preparation Note
Recommended storage: +2°C to +8°C.
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存储类别
12 - Non Combustible Liquids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
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