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N-Cadherin antibody (Extracellular Domain)

CDH2 Reactivity: Human WB, IF, FACS, BI Host: Mouse Monoclonal 8C11 unconjugated
Catalog No. ABIN967678
  • Target See all N-Cadherin (CDH2) Antibodies
    N-Cadherin (CDH2) (Cadherin 2 (CDH2))
    Binding Specificity
    • 22
    • 15
    • 14
    • 10
    • 6
    • 6
    • 4
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Extracellular Domain
    Reactivity
    • 134
    • 96
    • 68
    • 21
    • 16
    • 14
    • 8
    • 4
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Human
    Host
    • 88
    • 55
    • 4
    • 4
    • 3
    Mouse
    Clonality
    • 81
    • 73
    Monoclonal
    Conjugate
    • 88
    • 16
    • 5
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This N-Cadherin antibody is un-conjugated
    Application
    • 120
    • 58
    • 42
    • 40
    • 31
    • 23
    • 18
    • 15
    • 14
    • 13
    • 12
    • 8
    • 4
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunofluorescence (IF), Flow Cytometry (FACS), BioImaging (BI)
    Brand
    BD Pharmingen™
    Characteristics
    1. Since applications vary, each investigator should titrate the reagent to obtain optimal results.
    2. An isotype control should be used at the same concentration as the antibody of interest.
    3. Please refer to us for technical protocols.
    4. Sodium azide is a reversible inhibitor of oxidative metabolism, therefore, antibody preparations containing this preservative agent must not be used in cell cultures nor injected into animals. Sodium azide may be removed by washing stained cells or plate-bound antibody or dialyzing soluble antibody in sodium azide-free buffer. Since endotoxin may also affect the results of functional studies, we recommend the NA/LE (No Azide/Low Endotoxin) antibody format, if available, for in vitro and in vivo use.
    5. Caution: Sodium azide yields highly toxic hydrazoic acid under acidic conditions. Dilute azide compounds in running water before discarding to avoid accumulation of potentially explosive deposits in plumbing.
    Purification
    The monoclonal antibody was purified from tissue culture supernatant or ascites by affinity chromatography.
    Immunogen
    Human extracellular N-Cadherin domain Recombinant Protein
    Clone
    8C11
    Isotype
    IgG1 kappa
    Top Product
    Discover our top product CDH2 Primary Antibody
  • Application Notes
    Because the extracellular domain of N-Cadherin is trypsin-sensitive, it is important to avoid using trypsin to dissociate the cells to be studied.
    Comment

    Related Products: ABIN968535, ABIN967389

    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.5 mg/mL
    Buffer
    Aqueous buffered solution containing ≤0.09 % sodium azide.
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    4 °C
    Storage Comment
    Store undiluted at 4°C.
  • Wein, Pietsch, Saffrich, Wuchter, Walenda, Bork, Horn, Diehlmann, Eckstein, Ho, Wagner: "N-cadherin is expressed on human hematopoietic progenitor cells and mediates interaction with human mesenchymal stromal cells." in: Stem cell research, Vol. 4, Issue 2, pp. 129-39, (2010) (PubMed).

    Puch, Armeanu, Kibler, Johnson, Müller, Wheelock, Klein: "N-cadherin is developmentally regulated and functionally involved in early hematopoietic cell differentiation." in: Journal of cell science, Vol. 114, Issue Pt 8, pp. 1567-77, (2001) (PubMed).

    Knudsen, Soler, Johnson, Wheelock: "Interaction of alpha-actinin with the cadherin/catenin cell-cell adhesion complex via alpha-catenin." in: The Journal of cell biology, Vol. 130, Issue 1, pp. 67-77, (1995) (PubMed).

  • Target
    N-Cadherin (CDH2) (Cadherin 2 (CDH2))
    Alternative Name
    CD325 (CDH2 Products)
    Synonyms
    CD325 antibody, CDHN antibody, CDw325 antibody, NCAD antibody, N-cadherin antibody, cadherin-2 antibody, cdhn antibody, ncad antibody, cdw325 antibody, CDH2 antibody, Cadherin-2 antibody, Ncad antibody, glo antibody, lyr antibody, pac antibody, wu:fb47h04 antibody, cadherin 2 antibody, cadherin 2 S homeolog antibody, cadherin 2, type 1, N-cadherin (neuronal) antibody, CDH2 antibody, cdh2.S antibody, cdh2 antibody, Cdh2 antibody
    Background
    The 8C11 monoclonal antibody recognizes the extracellular domain of human N-Cadherin (CD325). Cadherins are a family of Ca2+ dependent intercellular adhesion molecules that play a central role in controlling morphogenetic movements during development. Their function is regulated by association with the actin cytoskeleton by a complex of cytoplasmic proteins called the catenins (alpha, beta, gamma). Members of the cadherin family include P-cadherin , E-cadherin (uvomorulin), N-cadherin (neural cadherin), R-cadherin, cadherin 5, L-CAM, and EP-cadherin. N-cadherin mRNA is found at elevated levels in brain and heart and at a much lower level in liver. Mechanisms such as mRNA expression, cytokine modulation, and protease-mediated turnover modulate N-cadherin protein levels during development. In addition, N-cadherin function is indirectly regulated by endogenous kinases and phosphatases. Tyrosine phosphorylation of beta-catenin complexed with N-cadherin results in dissociation of N-cadherin from actin. However, N-cadherin also interacts with a PTP1B-like phosphatase that dephosphorylates beta-catenin and promotes N-cadherin/actin association. Thus, N-cadherin is an integral adhesion molecule whose function is regulated by protein-protein interactions and phosphorylation/dephosphorylation events.
    Synonyms: Cadherin-2, N-Cadherin
    Molecular Weight
    130 kDa
    Gene ID
    1000
    Pathways
    Regulation of Muscle Cell Differentiation, Cell-Cell Junction Organization, Synaptic Membrane
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