MAB1950
Anti-Integrin α2 Antibody, clone P1E6
clone P1E6, Chemicon®, from mouse
Synonym(e):
CD49b
Anmeldenzur Ansicht organisationsspezifischer und vertraglich vereinbarter Preise
Alle Fotos(4)
About This Item
UNSPSC-Code:
12352203
eCl@ss:
32160702
NACRES:
NA.41
Biologische Quelle
mouse
Qualitätsniveau
Antikörperform
purified immunoglobulin
Antikörper-Produkttyp
primary antibodies
Klon
P1E6, monoclonal
Speziesreaktivität
human
Hersteller/Markenname
Chemicon®
Methode(n)
immunocytochemistry: suitable
immunohistochemistry: suitable
Isotyp
IgG1
Eignung
not suitable for immunohistochemistry (Paraffin)
NCBI-Hinterlegungsnummer
UniProt-Hinterlegungsnummer
Versandbedingung
wet ice
Posttranslationale Modifikation Target
unmodified
Angaben zum Gen
human ... ITGA2(3673)
Spezifität
Reacts with Human a2 integrin.
Anwendung
Research Category
Zellstruktur
Zellstruktur
Research Sub Category
Integrine
Integrine
Anti-Integrin α2 Antibody, clone P1E6 is an antibody against Integrin α2 for use in IC, IH.
Suitable for use in attachment inhibition assays using fibroblasts, epithelial cells, endothelial cells, and non-activated platelets on collagen types I, III, IV, VI and laminin.
Suitable for immunofluorescence using fresh frozen or acetone fixed tissues. Not recommended for traditional formalin fixed paraffin embedded tissues.
Final working dilutions must be determined by end user.
Suitable for immunofluorescence using fresh frozen or acetone fixed tissues. Not recommended for traditional formalin fixed paraffin embedded tissues.
Final working dilutions must be determined by end user.
Physikalische Form
Protein A purified
Format: Purified
Protein A Purified mouse immunoglobulin in 0.01 M phosphate buffered saline, pH 7.1, with 0.1% sodium azide as a preservative.
Lagerung und Haltbarkeit
Maintain for 1 year at 2–8°C from date of shipment. Aliquot to avoid repeated freezing and thawing. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
Hinweis zur Analyse
Control
Skin (Basement membrane)
Skin (Basement membrane)
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
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
10 - 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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Hirokazu Date et al.
Journal of orthopaedic research : official publication of the Orthopaedic Research Society, 28(2), 225-231 (2009-09-03)
Cellular activities responding to growth factors are important in ligament healing. The anterior cruciate ligament (ACL) has poor healing potential compared to the medial collateral ligament (MCL). To assess the differences, we investigated the proliferation, migration, adhesion, and matrix synthesis
Internalization of echovirus 1 in caveolae.
Marjomaki, V; Pietiainen, V; Matilainen, H; Upla, P; Ivaska, J; Nissinen, L; Reunanen et al.
Journal of virology null
N Théret et al.
Hepatology (Baltimore, Md.), 30(2), 462-468 (1999-07-27)
Fibrosis occurs in most chronic liver injuries and results from changes in the balance between synthesis and degradation of extracellular matrix components. In fibrotic livers, there is a markedly increased activity of matrix metalloproteinase 2 (MMP2), a major enzyme involved
Identification of P2Y12-dependent and -independent mechanisms of glycoprotein VI-mediated Rap1 activation in platelets.
Larson, MK; Chen, H; Kahn, ML; Taylor, AM; Fabre, JE; Mortensen, RM; Conley, PB; Parise, LV
Blood null
P D Arora et al.
The American journal of pathology, 154(3), 871-882 (1999-03-18)
Wound contraction is mediated by myofibroblasts, specialized fibroblasts that appear in large numbers as the wound matures and when resistance to contractile forces increases. We considered that the regulation of myofibroblast differentiation by wound-healing cytokines may be dependent on the
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