Compound | Cross-reactivity |
---|---|
cAMP | 100% |
ADP | <0.0001% |
ATP | <0.0001% |
GTP | <0.0001% |
cGMP | <0.0001% |
GDP | <0.0001% |
AMP | <0.0001% |
GMP | 0.00817% |
Competitive ELISA Protocol:
描述:小鼠抗cAMP單抗:抗cAMP小鼠單克隆抗體是GenScript提供的系列THE金牌抗體中的優(yōu)選抗體,是業(yè)內(nèi)高品質(zhì)的抗體之一。
品牌 | GenScript/金斯瑞 | 供貨周期 | 一周 |
---|---|---|---|
主要用途 | 用于尋找合適的腺苷酸環(huán)化酶激活劑或磷酸二酯酶抑制劑 | 應(yīng)用領(lǐng)域 | 醫(yī)療衛(wèi)生,食品,生物產(chǎn)業(yè),制藥 |
3ˊ,5ˊ-環(huán)腺苷酸(cyclic AMP,cAMP),是細(xì)胞膜上的一種特異性腺苷酸環(huán)化酶催化細(xì)胞內(nèi)的三磷酸腺苷(ATP)分解產(chǎn)生,是細(xì)胞內(nèi)重要的第二信使,參與信號轉(zhuǎn)導(dǎo)過程。cAMP調(diào)節(jié)關(guān)鍵的生理過程,包括代謝,分泌,鈣穩(wěn)態(tài),肌肉收縮,細(xì)胞命運(yùn)和基因轉(zhuǎn)錄等。和cAMP一樣,3ˊ,5ˊ-環(huán)鳥苷酸(cyclic GMP,cGMP),也是一種具有細(xì)胞內(nèi)信息傳遞作用的第二信使。它是由鳥苷酸環(huán)化酶(GC)分解GTP產(chǎn)生,可被G蛋白偶聯(lián)受體(G-protein linked receptor)激活的蛋白激酶(protein kinases)活化,進(jìn)而將胞外信號轉(zhuǎn)導(dǎo)至細(xì)胞核。環(huán)磷酸鳥苷(cGMP)可調(diào)節(jié)離子通道、糖原分解和細(xì)胞凋亡等。
抗cAMP小鼠單克隆抗體是GenScript提供的系列THE金牌抗體中的優(yōu)選抗體,是業(yè)內(nèi)高品質(zhì)的抗體之一。該抗體及相關(guān)的試劑盒已被廣泛用于藥物篩選研究中,用于尋找合適的腺苷酸環(huán)化酶激活劑或磷酸二酯酶抑制劑。高親和力的cAMP單克隆抗體,憑借靈敏度高,特異性好,批間穩(wěn)定性好,重復(fù)性好等優(yōu)勢,深受眾多科學(xué)家的認(rèn)可。
無非特異性反應(yīng)
靈敏度高于其他公司的同類產(chǎn)品
提供即用型的HRP偶聯(lián)的cAMP/cGMP
凍干粉在負(fù)20度及以下,可以保存至少2年
產(chǎn)品編號 | 名稱 | 數(shù)量 | 價(jià)格 | 操作 |
---|---|---|---|---|
A01509 | THE™ cAMP Antibody, mAb, Mouse | ¥2500.00 | ||
M01058 | cGMP-HRP | ¥1050.00200 μl | ||
M01059 | cAMP-HRP | ¥1050.00200 μl |
1. Cross Reactivity Analysis using THE™ cAMP Antibody (Mouse)(A01509)
Compound | Cross-reactivity |
---|---|
cAMP | 100% |
ADP | <0.0001% |
ATP | <0.0001% |
GTP | <0.0001% |
cGMP | <0.0001% |
GDP | <0.0001% |
AMP | <0.0001% |
GMP | 0.00817% |
Competitive ELISA Protocol:
ELISA plate was coated with goat anti-mouse IgG antibody.
THE™ cAMP Antibody(Mouse)(GenScript, A01509) at appropriate dulition and cAMP standards or testing compounds were added into appropriate reaction wells.
After a period of incubation, cAMP-HRP conjugate (GenScript, M01059) was added and developed at room temperature.
ELISA plate was washed with ELISA washing buffer, then TMB substrate was added and developed at room temperature.
Stop the reaction with 1.0 N HCl and read the plate at 450 nm.