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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

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

Source biologique

mouse

Niveau de qualité

100

Forme d'anticorps

purified antibody

Type de produit anticorps

primary antibodies

Clone

CH-11, monoclonal

Espèces réactives

human, mouse

Conditionnement

antibody small pack of 25 μg

Fabricant/nom de marque

Upstate®

Technique(s)

ELISA: suitable
immunocytochemistry: suitable
western blot: suitable

Isotype

IgG1

Numéro d'accès NCBI

NM_010612

Numéro d'accès UniProt

P35968

Conditions d'expédition

ambient

Modification post-traductionnelle de la cible

unmodified

Informations sur le gène

human ... KDR(3791)

Spécificité

KDR/Flk-1

Immunogène

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

Application

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.

Qualité

routinely evaluated by immunoblot on RIPA lysates from HUVEC cells

Description de la cible

230kDa

Forme physique

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

Autres remarques

Please refer to lot specific datasheet.

Informations légales

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

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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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Małgorzata Starek et al.
Molecules (Basel, Switzerland), 26(12) (2021-07-03)
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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