MAB2022
Anti-Keratan Sulfate Antibody, clone EFG-11
ascites fluid, clone EFG-11, Chemicon®
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About This Item
UNSPSCコード:
12352203
eCl@ss:
32160702
NACRES:
NA.41
クローン:
EFG-11, monoclonal
application:
ELISA
RIA
WB
RIA
WB
化学種の反応性:
sheep, bovine, pig, canine, mouse, human
テクニック:
ELISA: suitable
radioimmunoassay: suitable
western blot: suitable
radioimmunoassay: suitable
western blot: suitable
citations:
16
おすすめの製品
由来生物
mouse
品質水準
抗体製品の状態
ascites fluid
クローン
EFG-11, monoclonal
化学種の反応性
sheep, bovine, pig, canine, mouse, human
メーカー／製品名
Chemicon®
テクニック
ELISA: suitable
radioimmunoassay: suitable
western blot: suitable
アイソタイプ
IgG2b
NCBIアクセッション番号
UniProtアクセッション番号
輸送温度
dry ice
ターゲットの翻訳後修飾
unmodified
遺伝子情報
human ... LUM(4060)
特異性
Recognizes 2-3 disaccharide units on both skeletal (type II) and corneal (type I) keratan sulfate chains either in isolated or proteoglycan-bound form. The epitope is resistant to proteolytic or alkaline cleavages and partially sensitive to keratanase or other endo-B-galactosidase treatment.
免疫原
Human articular cartilage proteoglycan digested with chondroitinase ABC.
アプリケーション
Research Category
細胞骨格
細胞骨格
Research Sub Category
サイトケラチン
サイトケラチン
Anti-Keratan Sulfate Antibody, clone EFG-11 is an antibody against Keratan Sulfate for use in ELISA, RIA & WB.
Western blot at 1:1000 - 1:4000
ELISA at 1:5,000-1:20,000
RIA at 1:30,000-1:500,000
May be used in a competitive inhibition assay to measure keratan sulfate levels.
ELISA at 1:5,000-1:20,000
RIA at 1:30,000-1:500,000
May be used in a competitive inhibition assay to measure keratan sulfate levels.
物理的形状
Ascites liquid, no preservative.
保管および安定性
Maintain at -20°C in convenient aliquots for up to 12 months. Avoid repeated freeze/thaw cycles.
法的情報
CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany
免責事項
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.
保管分類コード
10 - Combustible liquids
WGK
WGK 1
引火点(°F)
Not applicable
引火点(℃)
Not applicable
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。
Jan Code
MAB2022:
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。
Jesús-José Ferre-Fernández et al.
Human genomics, 16(1), 49-49 (2022-10-27)
FOXC1 encodes a forkhead-domain transcription factor associated with several ocular disorders. Correct FOXC1 dosage is critical to normal development, yet the mechanisms controlling its expression remain unknown. Together with FOXQ1 and FOXF2, FOXC1 is part of a cluster of FOX
G Cs-Szabó et al.
Arthritis and rheumatism, 38(5), 660-668 (1995-05-01)
To identify characteristic changes in large aggregating (aggrecan) and small proteoglycan (PG) populations in articular cartilages during osteoarthritis (OA) and rheumatoid arthritis (RA). Aggrecan populations in guanidine extracts of femoral condylar cartilages of 46 OA and 8 RA patients who
Monoclonal antibodies to different protein-related epitopes of human articular cartilage proteoglycans.
Glant, T T, et al.
The Biochemical Journal, 234, 31-41 (1986)
Liping Yang et al.
Journal of the Association for Research in Otolaryngology : JARO, 19(4), 353-362 (2018-04-25)
Otoconia-related vertigo and balance deficits, particularly benign paroxysmal positional vertigo (BPPV), are common. Our recent studies in humans show that, while BPPV prevalence greatly increases with age in both genders, peri-menopausal women are especially susceptible. In the present study, we
Kathryn E Hendee et al.
Human molecular genetics, 27(10), 1675-1695 (2018-03-06)
The PITX2 (paired-like homeodomain 2) gene encodes a bicoid-like homeodomain transcription factor linked with several human disorders. The main associated congenital phenotype is Axenfeld-Rieger syndrome, type 1, an autosomal dominant condition characterized by variable defects in the anterior segment of
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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