추천 제품
결합
FITC conjugate
Quality Level
형태
buffered aqueous solution
농도
~20 mg/mL
저장 온도
2-8°C
타겟 번역 후 변형
unmodified
일반 설명
IgGs are glycoprotein antibodies that regulate immunological defense mechanisms such as phagocytosis and inflammatory responses . IgG also modulates complement-mediated cell lysis . IgG-FITC from human serum does not react with purified human IgA, IgG, IgM, and Bence Jones κ and lambda myeloma proteins. Additionally, the product does not react with serum from rat, goat, rabbit, guinea pig, and mouse.
애플리케이션
IgG-FITC from human serum is suitable for use in immunoaffinity purifications , and metal-enhanced fluorescence . The product may also be used for immunoelectrophoretic applications.
결합
Do not confuse with Anti-Human IgG–FITC conjugate.
물리적 형태
Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide
면책조항
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.
Storage Class Code
12 - Non Combustible Liquids
WGK
WGK 2
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
이미 열람한 고객
Selective nanopatterning of protein via ion-induced focusing and its application to metal-enhanced fluorescence.
Chang Gyu Woo et al.
Small (Weinheim an der Bergstrasse, Germany), 7(13), 1790-1794 (2011-05-14)
Purification of immunoglobulins from Serum Using Thiophilic Cellulose Beads
Subramanian, A.
International Journal of Biochromatography, 5(I), 31-47 (2000)
C I Bindon et al.
The Journal of experimental medicine, 168(1), 127-142 (1988-07-01)
Humanized antibodies are likely to have a major role in therapy and it is important to define their interaction with physiological effectors. By comparing a matched series of chimeric human mAbs we found that igG1 was most efficient in complement
Vishakha Sabharwal et al.
Infection and immunity, 77(3), 1121-1127 (2009-01-14)
Strategies to limit complement deposition on Streptococcus pneumoniae are established as virulence features for invasive disease, but their role in respiratory tract infection requires further analysis. We evaluated complement C3 protein deposition on discordant S. pneumoniae isolates of the same
Giovanni S Offeddu et al.
Small (Weinheim an der Bergstrasse, Germany), 15(46), e1902393-e1902393 (2019-09-10)
In vitro prediction of physiologically relevant transport of therapeutic molecules across the microcirculation represents an intriguing opportunity to predict efficacy in human populations. On-chip microvascular networks (MVNs) show physiologically relevant values of molecular permeability, yet like most systems, they lack
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