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Anti-ADAM10 antibody (ab1997)

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Overview

Product name

Anti-ADAM10 antibody
See all ADAM10 products (10) ...

Description

Rabbit polyclonal to ADAM10

Tested applications

IHC-P, WB, ELISA, ICC/IFmore details

Cross reactivity

Reacts with

Mouse, Human

Immunogen

Synthetic peptide, corresponding to amino acids 732-748 of Human ADAM10. This sequence is identical to those of bovine and rat origins and differs from that of mouse ADAM10 by one amino acid.

Epitope

PQRQRPRESYQMGHMRR

Positive control

Jurkat whole cell lysate

General notes

TNFa converting enzyme.

Properties

Form

Liquid

Storage instructions

Shipped at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.

Storage buffer

PBS with 0.02% sodium azide

Concentration

Concentration information loading...

Purity

Immunogen affinity purified

Clonality

Polyclonal

Isotype

IgG

  • Immunocytochemistry - ADAM10 antibody (ab1997)Immunocytochemistry - ADAM10 antibody (ab1997) image (enlarge)

  • Western blot - ADAM10 antibody (ab1997)Western blot - ADAM10 antibody (ab1997) image (enlarge)

  • Western blot - ADAM10 antibody (ab1997)Western blot - ADAM10 antibody (ab1997) image (enlarge)

Applications

Show applications key

Our Abpromise guarantee covers the use of ab1997 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

Target

Function

Cleaves the membrane-bound precursor of TNF-alpha at '76-Ala-
-Val-77' to its mature soluble form. Responsible for the proteolytical release of soluble JAM3 from endothelial cells surface. Responsible for the proteolytic release of several other cell-surface proteins, including heparin-binding epidermal growth-like factor, ephrin-A2 and for constitutive and regulated alpha-secretase cleavage of amyloid precursor protein (APP). Contributes to the normal cleavage of the cellular prion protein. Involved in the cleavage of the adhesion molecule L1 at the cell surface and in released membrane vesicles, suggesting a vesicle-based protease activity. Controls also the proteolytic processing of Notch and mediates lateral inhibition during neurogenesis.

Tissue specificity

Expressed in spleen, lymph node, thymus, peripheral blood leukocyte, bone marrow, cartilage, chondrocytes and fetal liver.

Sequence similarities

Contains 1 disintegrin domain.
Contains 1 peptidase M12B domain.

Domain

The conserved cysteine present in the cysteine-switch motif binds the catalytic zinc ion, thus inhibiting the enzyme. The dissociation of the cysteine from the zinc ion upon the activation-peptide release activates the enzyme.

Post-translational
modifications

The precursor is cleaved by a furin endopeptidase.

Cellular localization

Cell membrane. Endomembrane system. Is localized in the plasma membrane but is predominantly expressed in the Golgi apparatus and in released membrane vesicles derived likely from the Golgi.

Target information above from: UniProt accessionO14672 The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).

Information by UniProt

Alternative names

  • A disintegrin and metalloprotease domain 10 antibody
  • A Disintegrin And Metalloproteinase Domain 10 antibody
  • AD 10 antibody
  • AD10 antibody
  • ADA10_HUMAN antibody
  • ADAM 10 antibody
  • ADAM metallopeptidase domain 10 antibody
  • ADAM10 antibody
  • CD 156c antibody
  • CD156c antibody
  • CD156c antigen antibody
  • CDw156 antibody
  • disintegrin and metalloproteinase domain containing protein 10 antibody
  • Disintegrin and metalloproteinase domain-containing protein 10 antibody
  • HsT 18717 antibody
  • HsT18717 antibody
  • kuz antibody
  • kuzbanian antibody
  • Kuzbanian protein homolog antibody
  • MADM antibody
  • Mammalian disintegrin metalloprotease antibody
  • Mammalian disintegrin-metalloprotease antibody
see all

Anti-ADAM10 antibody images:

  Immunocytochemistry - ADAM10 antibody (ab1997)

Immunocytochemistry - ADAM10 antibody (ab1997)

ab1997 at 2µg/ml staining K562 cells by ICC/IF.

  Western blot - ADAM10 antibody (ab1997)

Western blot - ADAM10 antibody (ab1997)

All lanes : Anti-ADAM10 antibody (ab1997) at 1/1666 dilution

Lane 2 : ADAM10 siRNA treated human keratinocyte cells
Lane 3 : Non-treated human keratinocyte cells.

Secondary
HRP conjugated Goat anti-rabbit antibody
developed using the ECL technique

Performed under reducing conditions.

Predicted band size : 84 kDa
Observed band size : 75,100 kDa (why is the actual band size different from the predicted?)


Exposure time : 1 minute

This image is courtesy of an anonymous Abreview

See Abreview

  Western blot - ADAM10 antibody (ab1997)

Western blot - ADAM10 antibody (ab1997)

All lanes : Anti-ADAM10 antibody (ab1997) at 1/2000 dilution

Lane 1 : Jurkat whole cell lysate
Lane 2 : Jurkat whole cell lysate in presence of Blocking peptide at 1 µg/ml


Predicted band size : 84 kDa
Observed band size : 85 kDa (why is the actual band size different from the predicted?)

  Immunocytochemistry/ Immunofluorescence-ADAM10 antibody(ab1997)

Immunocytochemistry/ Immunofluorescence-ADAM10 antibody(ab1997)

ICC/IF image of ab1997 stained HeLa cells. The cells were 4% PFA fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab1997, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.

References for Anti-ADAM10 antibody (ab1997)

This product has been referenced in:

See all 8 publications for this product

Publishing research using ab1997? Please let us know so that we can cite the reference in this datasheet

Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"