SignalPlus抗体 Enhancer

目录号 GTX49999

文献引用 3

实验应用	WB, Dot, ELISA
产品包装	50 ml (¥2000)

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View product citations for antibody GTX49999 on CiteAb

产品说明

摘要

SignalPlus Antibody Enhancer for Western Blotting and ELISA enhances antigen-antibody reactions. SignalPlus Antibody Enhancer works well with chemiluminescence, colerimetric and fluorescence detection system. It can significantly enhance detection of weak immunoreactive and low abundance proteins in a variety of immunoassays such as Western blotting, dot blotting and ELISA. Simply dilute antibodies with SignalPlus Antibody Enhancer and process the rest of the procedures as usual. No additional steps are required. Signal enhancement is protein dependent and could vary from several folds to more than ten-fold.

产品应用

应用说明

Dilute primary antibody in Solution 1 and secondary antibody in Solution 2. We recommend using a 10-fold lower working concentration of primary antibody than is usually required for western blot. Optimal working dilutions should be determined experimentally by the end user.

产品属性

形式

Liquid

存放说明

Store at 4ºC.

注意事项

仅供实验室使用。不适用于人类或动物的任何临床，治疗或诊断用途。不适合动物或人类食用。

產品图片

GTX49999 Dot Image

Antibody diluted in SignalPlus Antibody Enhancer solution can detect more than 100-fold lower levels of antigen than antibody diluted in standard buffers

GTX49999 WB Image

Antibody diluted in SignalPlus Antibody Enhancer solution has superior signal to antibody diluted in standard buffers, even at a 10-fold lower concentration of antibody.

GTX49999 WB Image

Detection enhancement of Rac1 with treatment of Signal + in Western blot. Treatment with GTX49999 resulted in clear signal, whereas dilution with conventional PBS-T resulted in no signal. Primary Ab: Anti-Rac1 (1: 1,000) Secondary Ab: Anti-Mouse IgG-HRP (1: 2,500) Sample: Rat cortical primary neuron Detection: ECL

GTX49999 WB Image

Detection enhancement of pJNK with treatment of Signal + in Western blot. Treatment with GTX49999 resulted in clear signal enhancement and background suppression compared with the conventional method using TBS-T. Primary Ab: Anti-pJNK (1: 1,000) Secondary Ab: Anti-rabbit IgG - HRP (1: 5,000) Sample: Mouse Embryonic Fibroblast (MEF) Detection: SuperSignal West Pico

文献引用

Application Reference

GDULA-ARGASINSKA J et al. Acta Poloniae Pharmaceutica 2018; 75 (2) : 423-433 ANTI-INFLAMMATORY PROPERTIES OF CANTHARELLUS CIBARIUS FROM IN VITRO CULTURE ENRICHED IN ZINC.

Gdula-Argasi?ska J et al. Acta Biochim Pol 2017; 64 (3) : 551-559 Anti-inflammatory activities of garlic sprouts, a source of α-linolenic acid and 5-hydroxy-l-tryptophan, in RAW 264.7 cells.

Joanna Gdula-Argasin’ ska et al. Pharmacol Rep. 2015; 67 (3) : 610-5 n-3 fatty acids as resolvents of inflammation in the A549 cells.

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Application Reference

GDULA-ARGASINSKA J et al. Acta Poloniae Pharmaceutica 2018; 75 (2):423-433 ANTI-INFLAMMATORY PROPERTIES OF CANTHARELLUS CIBARIUS FROM IN VITRO CULTURE ENRICHED IN ZINC.

Gdula-Argasi?ska J et al. Acta Biochim Pol 2017; 64 (3):551-559 Anti-inflammatory activities of garlic sprouts, a source of α-linolenic acid and 5-hydroxy-l-tryptophan, in RAW 264.7 cells.

Joanna Gdula-Argasin’ ska et al. Pharmacol Rep. 2015; 67 (3):610-5 n-3 fatty acids as resolvents of inflammation in the A549 cells.

Document
Phosphorylated.pdf

产品包装

报价 (¥)

50 ml

¥ 2000

Qty

SignalPlus抗体 Enhancer

目录号 GTX49999

实验应用

摘要

产品应用

应用说明

产品属性

形式

存放说明

注意事项

產品图片

GTX49999 Dot Image

GTX49999 WB Image

GTX49999 WB Image

GTX49999 WB Image

文献引用

Application Reference

产品评论

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