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MAB3321

Sigma-Aldrich

Anti-MMP-13 Antibody, clone 181-15A12

clone 181-15A12, Chemicon®, from mouse

Synonym(e):

Collagenase-3

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About This Item

UNSPSC-Code:
12352203
eCl@ss:
32160702
NACRES:
NA.41

Biologische Quelle

mouse

Qualitätsniveau

Antikörperform

purified immunoglobulin

Antikörper-Produkttyp

primary antibodies

Klon

181-15A12, monoclonal

Speziesreaktivität

human

Hersteller/Markenname

Chemicon®

Methode(n)

ELISA: suitable
immunohistochemistry: suitable (paraffin)
western blot: suitable

Isotyp

IgG1κ

NCBI-Hinterlegungsnummer

UniProt-Hinterlegungsnummer

Versandbedingung

dry ice

Posttranslationale Modifikation Target

unmodified

Angaben zum Gen

human ... MMP13(4322)

Verwandte Kategorien

Spezifität

Reacts with precursor and active forms of human MMP-13 and does not cross-react with human MMP-1, 2, 3, 7, 8, 9. This is a purified mouse moncolonal antibody to recombinant human matrix metalloproteinase 13 (human MMP-13, procollagenase-3).

Anwendung

Research Category
Zellstruktur
Research Sub Category
MMPs & TIMPs
Anti-MMP-13 Antibody, clone 181-15A12 detects level of MMP-13 & has been published & validated for use in ELISA, WB, IH(P).
Immunoblotting

Immunohistochemistry on paraffin-embedded tissue sections.

Physikalische Form

Format: Purified
Purified immunoglobulin to recombinant human matrix metalloproteinase 13 (human MMP-13, procollagenase-3). Liquid in 0.1 M PBS, pH 7.0 containing 4% protease free bovine serum albumin.

Lagerung und Haltbarkeit

Maintain at -20°C for up to 12 months from date of receipt. Avoid repeated freeze/thaw cycles.

Sonstige Hinweise

Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.

Rechtliche Hinweise

CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany

Haftungsausschluss

Manufactured by Daiichi Fine Chemical Co., Ltd

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.

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Lagerklassenschlüssel

12 - Non Combustible Liquids

WGK

WGK 2

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Die Dokumentenbibliothek aufrufen

Development of a solid-phase assay for analysis of matrix metalloproteinase activity.
Lauer-Fields, JL; Nagase, H; Fields, GB
Journal of biomolecular techniques : JBT null
M R Junttila et al.
Oncogene, 26(36), 5267-5279 (2007-03-06)
Recent studies indicate that the specificity of p38 mitogen-activated protein kinase (MAPK)-mediated cellular stress responses is determined by the expression pattern of the distinct p38 isoforms. Here, we have analysed the function of distinct p38 isoforms in the growth and
J M Del Casar et al.
Breast cancer research and treatment, 116(1), 39-52 (2009-02-26)
An immunohistochemical study was performed using tissue arrays and specific antibodies against MMPs -1, -2, -7, -9, -11, -13, -14, and TIMPs -1, -2 and -3. More than 5,000 determinations on cancer specimens from 124 patients with invasive breast cancer
Jorge González-Zamora et al.
Antioxidants (Basel, Switzerland), 12(4) (2023-04-28)
Age-related macular degeneration (AMD) is a leading cause of severe vision loss in older individuals in developed countries. Despite advances in our understanding of AMD, its pathophysiology remains poorly understood. Matrix metalloproteinases (MMPs) have been proposed to play a role
Elizabeth H Stephens et al.
Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society, 13(6), 447-458 (2010-06-12)
At birth, the mechanical environment of valves changes radically as fetal shunts close and pulmonary and systemic vascular resistances change. Given that valves are reported to be mechanosensitive, we investigated remodeling induced by perinatal changes by examining compositional and structural

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