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14-734-M

Sigma-Aldrich

FGFR1 (V561M) Protein, active, 10 µg

Active, N-terminal GST-tagged, recombinant, human FGFR1 amino acids 456 -765 containing the V561 mutation. For use in Enzyme Assays.

Synonyme(s) :

Basic Fibroblast Growth Factor Receptor 1, c-fgr, CD331

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About This Item

Code UNSPSC :
12352202
eCl@ss :
32160405
Nomenclature NACRES :
NA.32

Source biologique

human

Niveau de qualité

Produit recombinant

expressed in baculovirus infected Sf21 cells

Poids mol.

Mw 62.3 kDa

Fabricant/nom de marque

Upstate®

Technique(s)

activity assay: suitable

Numéro d'accès UniProt

Informations sur le gène

human ... FGFR1(2260)

Description générale

N-terminal GST-tagged, recombinant, human FGFR1 amino acids 456 - 765 containing the V561 mutation. The coordinates for recombinant human FGFR1 were described in Homann et al. (2001). Blencke et al. (2004) suggested mutations to a conserved threonine residue at the ATP binding site would result in inhibitor resistance. The amino acid valine 561 was mutated to a methionine in FGFR1 which corresponded to previously reported mutations found in Abl (T315) and EGFR (T766) which had been shown to confer resistance to selective inhibitors. Assay data for FGFR1 V561M had shown that this mutation had conferred resistance to PP58 (pyrido [2,3-d] pyrimidine tyrosine kinase inhibitor) compared to that of the wild type.
Product Source: Recombinant human FGFR1 expressed by baculovirus in Sf21 cells.

Application

Research Category
Metabolism
Research Sub Category
Obesity

Metabolic Disorders

Actions biochimiques/physiologiques

Protein Target: FGFR1
Target Sub-Family: TK

Qualité

Routinely evaluated by phosphorylation of 500μM GGEEEEYFELVKKKK

Forme physique

Glutathione-agarose
Presented as a frozen solution in 50mM Tris/HCl pH 7.5, 300mM NaCl, 0.1mM EGTA, 0.03% Brij 35, 270mM sucrose, 1mM benzamidine, 0.2mM PMSF, 0.1% 2-mercaptoethanol.

Stockage et stabilité

Stable for 6 months at -70°C from date of shipment. Upon first use, rapidly thaw the vial under cold water and immediately place on ice. Aliquot unused material into pre-chilled microcentrifuge tubes and immediately snap-freeze the vials in liquid nitrogen prior to re-storage at -70°C.

Autres remarques

Concentration: Please see lot specific Certificarte of Analysis.
For Specific Activity data, refer to the Certificate of Analysis for individual lots of this enzyme.
Please see lot specific Certificarte of Analysis.

Informations légales

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

Clause de non-responsabilité

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.

Pictogrammes

Exclamation mark

Mention d'avertissement

Warning

Mentions de danger

Classification des risques

Skin Sens. 1

Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

S Homann et al.
Journal of biotechnology, 86(1), 51-58 (2001-02-27)
When tumors undergo the angiogenic switch, cell growth and tissue invasion is facilitated by the formation of new capillaries from preexisting blood vessels, a process known as angiogenesis. Growth factors such as vascular endothelial growth factor/vascular permeability factor (VEGF/VPF) and
Characterization of a conserved structural determinant controlling protein kinase sensitivity to selective inhibitors.
Blencke S, Zech B, Engkvist O, Greff Z, Orfi L, Horvath Z, Keri G, Ullrich A, Daub H.
Chemistry and Biology, 5, 691-701 (2004)

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