Mouse myeloma cell line NS0-derived recombinant human ADAM9 Ectodomain Accession # Q13443
Specificity
Detects human ADAM9 Ectodomain in Western blots. In Western blots, approximately 10% cross-reactivity with the ectodomain of recombinant mouse ADAM9 is observed and no cross-reactivity with the ectodomain of recombinant human ADAM8, 9, 15, or 17 is observed.
Source
N/A
Isotype
IgG1
Clonality
Monoclonal
Host
Mouse
Gene
ADAM9
Purity Statement
Protein A or G purified from hybridoma culture supernatant
Innovator's Reward
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Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
12 months from date of receipt, -20 to -70 °C as supplied.
1 month, 2 to 8 °C under sterile conditions after reconstitution.
6 months, -20 to -70 °C under sterile conditions after reconstitution.
Buffer
Lyophilized from a 0.2 μm filtered solution in PBS with Trehalose. *Small pack size (SP) is supplied either lyophilized or as a 0.2 µm filtered solution in PBS.
Preservative
No Preservative
Reconstitution Instructions
Reconstitute at 0.5 mg/mL in sterile PBS.
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for ADAM9 Antibody (138537) [Unconjugated]
a disintegrin and metalloproteinase domain 9 (meltrin gamma)
ADAM 9
ADAM metallopeptidase domain 9 (meltrin gamma)
ADAM metallopeptidase domain 9
ADAM9
Cellular disintegrin-related protein
cone rod dystrophy 9
CORD9
disintegrin and metalloproteinase domain-containing protein 9
EC 3.4.24
EC 3.4.24.-
MCMP
MCMPMDC9KIAA0021Mltng
MDC9
Meltrin gamma
Meltrin-gamma
Metalloprotease/disintegrin/cysteine-rich protein 9
MLTNG
Myeloma cell metalloproteinase
Background
ADAM9, also known as MDC9 or meltrin gamma , is a member of the ADAM family that contains a disintegrin and metalloprotease-like domain (1). Like other membrane-anchored ADAMs, ADAM9 consists of a pro domain with a cysteine switch and furin cleavage sequence, a catalytic domain with the zinc-binding site and Met-turn expected for reprolysins, a disintegrin-like domain, a cysteine-rich domain, an EGF-like domain, a transmembrane domain, and the cytoplasmic domain. ADAM9 is able to cleave peptides corresponding to cleavage sites of tumor necrosis factor-alpha (TNF-alpha ), the p75 TNF receptor, the beta -amyloid protein precursor, and the c-kit ligand-1, implying that it may participate in shedding of these membrane proteins (2). In fact, ADAM9 has been shown to shed membrane-anchored heparin-binding EGF-like growth factor (3). In addition, it also cleaves oxidized insulin beta -chain and fibronectin (2,4). Besides its catalytic activity, ADAM9 functions as an adhesion molecule through binding of its disintegrin domain to integrins such as alpha v beta 5 and alpha 6 beta 1 (5, 6). The cytoplasmic domain of ADAM9 interacts with Src homology 3 (SH3)‑containing proteins and protein kinase C, and may mediate different signaling pathways (3, 7). ADAM9 is widely expressed in tissues (8).
Moss, et al. (2001) DDT 6:417.
Roghan, et al. (1999) J. Biol. Chem. 274:3531.
Izumi, et al. (1998) EMBO J. 17:7260.
Schwettmann and Tschesche (2001) Prot. Expre. & Purif. 21:65.
Nath, et al. (2000) J. Cell Sci. 113:2319.
Zhou, et al. (2001) Biochem. Biophys. Res. Comm. 280:574.
Howard, et al. (1999) J. Biol. Chem. 274:31693.
Weskamp, et al. (1996) J. Cell. Biol. 132:717.
Limitations
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.
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