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Merck
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主要文件

B2901

Sigma-Aldrich

抗-牛血清白蛋白抗体 小鼠抗

clone BSA-33, ascites fluid

别名:

抗-BSA, 抗-白蛋白,牛血清

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About This Item

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

生物源

mouse

共軛

unconjugated

抗體表格

ascites fluid

抗體產品種類

primary antibodies

無性繁殖

BSA-33, monoclonal

包含

15 mM sodium azide

物種活性

bovine (high), turkey (low), canine (low), sheep (high), horse (low), goat (high)

應無反應活性

human, hamster, rabbit, donkey, guinea pig, mouse, rat, chicken, feline, pigeon, pig

技術

dot blot: suitable
indirect ELISA: 1:1,000

同型

IgG2a

運輸包裝

dry ice

儲存溫度

−20°C

目標翻譯後修改

unmodified

基因資訊

bovine ... Alb(280717)
chicken ... Alb(396197)
dog ... Alb(403550)
horse ... Alb(100034206)
human ... ALB(213)
mouse ... Alb(11657)
pig ... Alb(396960)
rabbit ... Alb(100009195)
rat ... Alb(24186)
sheep ... Alb(443393)

一般說明

牛血清白蛋白(BSA)是一种66kDa的α-螺旋、球状、非糖基化蛋白。具有三个结构域,每个均带有两个亚结构域。属于血清白蛋白家族,具有17个二硫键。

特異性

牛血清白蛋白(BSA)在肝脏中合成,是血清中的主要蛋白,占比超过50%。
抗牛血清白蛋白单克隆抗体特异性针对SDS变性和还原BSA。本品与山羊和绵羊血清具有强交叉反应性,但与狗、火鸡和马血清白蛋白的亲和性较低。

免疫原

牛血清白蛋白

應用

抗牛血清白蛋白单克隆抗体可用于:
  • 酶联免疫吸附试验(ELISA)
  • 竞争性ELISA
  • 免疫印迹法
  • 蛋白质印迹
  • 从生物体液中免疫亲和纯化或吸附BSA

生化/生理作用

本牛血清白蛋白(BSA)常用作蛋白标准品,也可用于细胞培养基、司法鉴定和食品制作。它还可充当药物、激素和脂肪酸的转运蛋白。

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人类或动物食用或应用。

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儲存類別代碼

12 - Non Combustible Liquids

水污染物質分類(WGK)

nwg

閃點(°F)

Not applicable

閃點(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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J T Belisle et al.
Journal of bacteriology, 176(8), 2151-2157 (1994-04-01)
A fundamental ultrastructural feature shared by the spirochetal pathogens Treponema pallidum subsp. pallidum (T. pallidum) and Borrelia burgdorferi, the etiological agents of venereal syphilis and Lyme disease, respectively, is that their most abundant membrane proteins contain covalently attached fatty acids.
Marie Louise Gross et al.
Kidney international, 62(1), 51-59 (2002-06-26)
A substantial body of experimental evidence suggests that protein loading causes activation of proximal tubular epithelial cells with consecutive interstitial fibrosis. These studies have mostly been performed using mammalian in vivo models of glomerular damage or tissue cultures of mammalian
W Ye et al.
The Journal of biological chemistry, 270(18), 10933-10939 (1995-05-05)
We separately expressed the 58-kDa C-terminal, 42-kDa middle, 16-kDa C-terminal, and 33-kDa N-terminal regions of AP-3 (also called F1-20, AP180, NP185, and pp155), and determined their clathrin binding and assembly properties. The 58-kDa C-terminal region of AP-3 is able to
David W Nees et al.
Investigative ophthalmology & visual science, 44(8), 3339-3345 (2003-07-29)
To compare the abundance and spatial distribution of serum albumin in the mouse and bovine cornea. Serum albumin from cornea was separated from transketolase by SDS-PAGE (+/-dithiothreitol [DTT]) and identified by peptide sequencing and immunoblot analyses. The fractional content of
M A Callahan et al.
The Journal of biological chemistry, 276(30), 28022-28028 (2001-05-29)
During the course of the transmissible spongiform encephalopathy diseases, a protease-resistant ordered aggregate of scrapie prion protein (PrP(Sc)) accumulates in affected animals. From mechanistic and therapeutic points of view, it is relevant to determine the extent to which PrP(Sc) formation

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