跳转至内容
Merck

F9636

Sigma-Aldrich

IgG−FITC 来源于人类血清

~20 mg/mL, buffered aqueous solution

别名:

IgG-Fluorescein isothiocyanate from human serum

登录查看公司和协议定价


About This Item

MDL號碼:
分類程式碼代碼:
12352203
NACRES:
NA.46

共軛

FITC conjugate

品質等級

形狀

buffered aqueous solution

濃度

~20 mg/mL

儲存溫度

2-8°C

目標翻譯後修改

unmodified

一般說明

IgG 是糖蛋白抗体,可调节吞噬作用和炎症反应等免疫防御机制 。IgG 也可调节补体介导的细胞溶解 。来自人血清的 IgG-FITC 不与纯化的人 IgA、IgG、IgM 和 Bence Jonesκ 反应骨髓瘤蛋白和 λ 骨髓瘤蛋白。此外,本品不与大鼠、山羊、兔、豚鼠和小鼠的血清反应。

應用

人血清中的 IgG-FITC 适用于免疫亲和纯化 和金属增强荧光 。该产品也可用于免疫电泳应用。

聯結

不要与抗人 IgG–FITC 结合物混淆。

外觀

溶于含有15 mM叠氮化钠的0.01 M磷酸盐缓冲液(pH 7.4)

免責聲明

除非我们的产品目录或产品附带的其他公司文档另有说明,否则我们的产品仅供研究使用,不得用于任何其他目的,包括但不限于未经授权的商业用途、体外诊断用途、离体或体内治疗用途或任何类型的消费或应用于人类或动物。

儲存類別代碼

12 - Non Combustible Liquids

水污染物質分類(WGK)

WGK 2

閃點(°F)

Not applicable

閃點(°C)

Not applicable


分析证书(COA)

输入产品批号来搜索 分析证书(COA) 。批号可以在产品标签上"批“ (Lot或Batch)字后找到。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

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

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门