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Merck
CN

MAB3482

抗囊性纤维化跨膜电导调节剂抗体,克隆MM13-4

clone MM13-4, Chemicon®, from mouse

别名:

CFTR

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关于此项目

UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
Conjugate:
unconjugated
Clone:
MM13-4, monoclonal
Application:
ICC, IP, WB
Citations:
27
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biological source

mouse

Quality Level

conjugate

unconjugated

antibody form

purified immunoglobulin

antibody product type

primary antibodies

clone

MM13-4, monoclonal

species reactivity

human

should not react with

mouse, shark

manufacturer/tradename

Chemicon®

technique(s)

immunocytochemistry: suitable, immunoprecipitation (IP): suitable, western blot: suitable

isotype

IgG1

NCBI accession no.

UniProt accession no.

shipped in

wet ice

target post-translational modification

unmodified

Gene Information

human ... CFTR(1080)

Immunogen

合成肽(RKGYRQRLELSD),对应于人囊性纤维化跨膜传导调节蛋白(CFTR)的残基25-36。

Application

使用经验证用于IC、IP & WB的抗囊性纤维化跨膜传导调节蛋白抗体(克隆MM13-4)检测囊性纤维化跨膜传导调节蛋白。
研究子类别
离子通道 & 转运蛋白
研究类别
神经科学
蛋白质印迹:10 μg/mL,可识别CFTR(150-170kDa)和另外两个52kDa和38kDa的蛋白

免疫沉淀

免疫荧光

注意:在石蜡包埋组织上不起作用。

最佳工作稀释度必须由最终用户进行确定。

Biochem/physiol Actions

人囊性纤维化跨膜传导调节蛋白(CFTR)。识别残基24和35之间的N端表位。

Physical form

形式:纯化
纯化的免疫球蛋白。 液体形式,溶于0.02 M磷酸盐缓冲液、0.25 M NaCl(pH 7.6)和0.1%叠氮化钠中。

Preparation Note

以未稀释等分试样保存于2-8°C下6个月。

Other Notes

浓度:请参考批次特异性浓缩物的检验报告。

Legal Information

CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

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。


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存储类别

12 - Non Combustible Liquids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable



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Chunying Li et al.
The Journal of biological chemistry, 279(23), 24673-24684 (2004-04-03)
Based on electrophysiological measurements, it has been argued that the active form of cystic fibrosis trans-membrane conductance regulator (CFTR) Cl(-) channel is a multimer. It has also been demonstrated that this multimerization is likely due to PDZ domain-interacting partners. Here
Hong Yu Ren et al.
Molecular biology of the cell, 24(19), 3016-3024 (2013-08-09)
Cystic fibrosis (CF) is a fatal genetic disorder associated with defective hydration of lung airways due to the loss of chloride transport through the CF transmembrane conductance regulator protein (CFTR). CFTR contains two membrane-spanning domains (MSDs), two nucleotide-binding domains (NBDs)
Lianwu Fu et al.
The Biochemical journal, 441(2), 633-643 (2011-10-15)
CFTR (cystic fibrosis transmembrane conductance regulator) is expressed in the apical membrane of epithelial cells. Cell-surface CFTR levels are regulated by endocytosis and recycling. A number of adaptor proteins including AP-2 (μ2 subunit) and Dab2 (Disabled-2) have been proposed to



全球贸易项目编号

货号GTIN
MAB348204053252467929