2. Neuronal Signaling
  3. α-synuclein
  4. Prasinezumab

Prasinezumab  (Synonyms: PRX 002; RG 7935; RO 7046015)

目录号: HY-P99405 纯度: 99.90%
COA

摩尔计算器

Prasinezumab (PRX 002) 是一种针对聚集的 α-突触核蛋白 (α-synuclein) 的人源化 IgG1 单克隆抗体。Prasinezumab 具有用于帕金森病研究的潜力。

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Prasinezumab Chemical Structure

Prasinezumab Chemical Structure

CAS No. : 1960462-19-4

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规格 价格 是否有货 数量
1 mg ￥3400
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5 mg ￥9800
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Prasinezumab 相关抗体

Top Publications Citing Use of Products

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Prasinezumab (PRX 002) is a humanized IgG1 monoclonal antibody directed against aggregated α-synuclein. Prasinezumab has the potential for Parkinson's disease research[1].

体外研究
(In Vitro)

Prasinezumab 针对人 α-突触核蛋白羧基末端的表位。 Prasinezumab 以高亲和力与人类聚集的 α-突触核蛋白结合[1]。

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

Prasinezumab 相关抗体:
Clinical Trial
CAS 号
性状

液体

颜色

Colorless to light yellow

中文名称

普尼珠单抗
运输条件

Shipping with dry ice.
储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.
纯度 & 产品资料
参考文献

Prasinezumab 相关分类

  • 摩尔计算器

  • 稀释计算器

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

质量   浓度   体积   分子量 *
= × ×

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start) × 体积 (start) = 浓度 (final) × 体积 (final)
× = ×
C1   V1   C2   V2
Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

Keywords:

Prasinezumab1960462-19-4PRX 002 RG 7935 RO 7046015普尼珠单抗PRX002PRX-002RG7935RG 7935RG-7935RO7046015RO 7046015RO-7046015α-synucleinα-Synhumanized IgG1 monoclonal antibodyParkinson's diseaseInhibitorinhibitorinhibit

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