05-554
Anti-KDR/Flk-1/VEGFR2 Antibody, clone CH-11
clone CH-11, Upstate®, from mouse
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この商品について
UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
Conjugate:
unconjugated
Clone:
CH-11, monoclonal
Application:
ELISA, ICC, WB
Citations:
32
biological source
mouse
Quality Level
conjugate
unconjugated
antibody form
purified antibody
antibody product type
primary antibodies
clone
CH-11, monoclonal
species reactivity
human, mouse
packaging
antibody small pack of 25 μg
manufacturer/tradename
Upstate®
technique(s)
ELISA: suitable, immunocytochemistry: suitable, western blot: suitable
isotype
IgG1
NCBI accession no.
UniProt accession no.
shipped in
ambient
target post-translational modification
unmodified
Gene Information
human ... KDR(3791)
関連するカテゴリー
General description
230kDa
Immunogen
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.
Biochem/physiol Actions
KDR/Flk-1
Physical form
20mM sodium phosphate, pH 7.6, 250mM NaCl with 0.1% sodium azide
Format: Purified
Analysis Note
routinely evaluated by immunoblot on RIPA lysates from HUVEC cells
Other Notes
Please refer to lot specific datasheet.
Legal Information
UPSTATE is a registered trademark of Merck KGaA, Darmstadt, Germany
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WGK 2
保管分類
12 - Non Combustible Liquids
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
05-554-25UG: + 05-554:
jan
試験成績書（COA）
製品のロット番号・バッチ番号を入力して、試験成績書（COA） を検索できます。ロット番号・バッチ番号は、製品ラベルに「Lot」または「Batch」に続いて記載されています。
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
グローバルトレードアイテム番号
| カタログ番号 | GTIN |
|---|---|
| 05-554 | 04053252728396 |
| 05-554-25UG | 04054839342394 |
ライフサイエンス、有機合成、材料科学、クロマトグラフィー、分析など、あらゆる分野の研究に経験のあるメンバーがおります。.
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