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Merck
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Key Documents

05-554

Sigma-Aldrich

Anti-KDR/Flk-1/VEGFR2 Antibody, clone CH-11

clone CH-11, Upstate®, from mouse

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About This Item

Codice UNSPSC:
12352203
eCl@ss:
32160702
NACRES:
NA.41

Origine biologica

mouse

Livello qualitativo

100

Forma dell’anticorpo

purified antibody

Tipo di anticorpo

primary antibodies

Clone

CH-11, monoclonal

Reattività contro le specie

human, mouse

Confezionamento

antibody small pack of 25 μg

Produttore/marchio commerciale

Upstate®

tecniche

ELISA: suitable
immunocytochemistry: suitable
western blot: suitable

Isotipo

IgG1

N° accesso NCBI

NM_010612

N° accesso UniProt

P35968

Condizioni di spedizione

ambient

modifica post-traduzionali bersaglio

unmodified

Informazioni sul gene

human ... KDR(3791)

Specificità

KDR/Flk-1

Immunogeno

Recombinant protein corresponding to residues 1158-1345 of murine KDR/Flk-1

Applicazioni

Anti-KDR/Flk-1/VEGFR2 Antibody, clone CH-11 detects level of KDR/Flk-1/VEGFR2 & has been published & validated for use in ELISA, IC & WB.

Qualità

routinely evaluated by immunoblot on RIPA lysates from HUVEC cells

Descrizione del bersaglio

230kDa

Stato fisico

20mM sodium phosphate, pH 7.6, 250mM NaCl with 0.1% sodium azide
Format: Purified

Altre note

Please refer to lot specific datasheet.

Note legali

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

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Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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Metronidazole is a drug widely used in the prevention and treatment of bacterial infections. Due to its possibility of the formation of stable metal complexes, it was decided to broaden its activity spectrum by introducing the silver(I) coordination compounds i.e.
Ashok Aspatwar et al.
Journal of enzyme inhibition and medicinal chemistry, 35(1), 109-117 (2019-11-07)
With the aim to obtain novel compounds possessing both strong affinity against human carbonic anhydrases and low toxicity, we synthesised novel thiourea and sulphonamide derivatives 3, 4 and 10, and studied their in vitro inhibitory properties against human CA I, CA
Pelayo Camps et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 21(40), 14036-14046 (2015-09-17)
Two domino Diels-Alder adducts were obtained from 3,7-bis(cyclopenta-2,4-dien-1-ylidene)-cis-bicyclo[3.3.0]octane and dimethyl acetylenedicarboxylate or N-methylmaleimide under microwave irradiation. From the first adduct, a C20H24 diene with C2v symmetry was obtained by Zn/AcOH reduction, hydrolysis, oxidative decarboxylation, and selective hydrogenation. Photochemical [2+2] cycloaddition
Nikola Burdzhiev et al.
Molecules (Basel, Switzerland), 25(17) (2020-08-23)
Tautomerization of 2-phenylimidazolecarbaldehydes has not been studied in detail so far, although this process is a well-known phenomenon for imidazole derivatives. That is why we focus our study on a series of 2-phenylimidazolecarbaldehydes and their parent alcohols that were synthesized
Rebecca R Foster et al.
The American journal of pathology, 173(4), 938-948 (2008-09-06)
We have previously reported expression of vascular endothelial growth factor (VEGF)-A and -C in glomerular podocytes and actions of VEGF-A on glomerular endothelial cells (GEnC) that express VEGF receptor-2 (VEGFR-2). Here we define VEGFR-3 expression in GEnC and investigate the
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