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產(chǎn)品資料

Vedolizumab

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產(chǎn)品名稱: Vedolizumab
產(chǎn)品型號(hào): PHM220227
產(chǎn)品展商: 晶欣生物
產(chǎn)品文檔:
 Vedolizumab Clinical Trial

產(chǎn)品簡(jiǎn)介使用說(shuō)明產(chǎn)品圖片相關(guān)產(chǎn)品相關(guān)論文

產(chǎn)品參數(shù)

品  名

貨  號(hào)

CAS 號(hào)

純  度

規(guī)  格

價(jià)格

Vedolizumab

PHM220227

943609-66-3

99.64%

1 mg

4000

5 mg

7400

25mg

28000

50 mg

45000

產(chǎn)品簡(jiǎn)介

Vedolizumab是一種靶向α4β7整聯(lián)蛋白 (integrin) 的人源化單克隆抗體,用于潰瘍性結(jié)腸炎和克羅恩病的相關(guān)研究。

詳細(xì)介紹

生物活性

Bevacizumab, a humanized monoclonal antibody, specifically binds to all VEGF-A isoforms with high affinity.

IC50 & Target

VEGF

體外研究
(In Vitro)

Bevacizumab, a humanized monoclonal antibody, specifically binds to all VEGF-A isoforms with high affinity,

and inhibits its interaction with VEGFR-1 and VEGFR-2. Experimental analysis shows that the EC50

ofBevacizumab to bind VEGF analyzed by ELISA is 0.18 μg/mL. Binding kinetics assays show similar results

that Bevacizumab inhibits the VEGF-induced proliferation of HUVEC with an IC50 value of 0.047±0.0081 μg/mL.

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

體內(nèi)研究
(In Vivo)

It is demonstrated that the subconjunctival administration of FD006 and Bevacizumab can

significantly inhibit CoNV in NaOH cauterized rats compared with the control group (p?<?0.01)

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

149 kDa(Average)

CAS號(hào)

216974-75-3

中文名稱

貝伐珠單抗

儲(chǔ)存方式

Please store the product under the recommended conditions in the Certificate of Analysis.



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