Glutathione (GSH/GSSG/Total) Fluorometric Assay Kit.

Kit Summary:

• Detection method- Fluorescence (Ex/Em 340/420 nm)

• Sample type- Cell and Tissue lysates, culture media, urine, plasma and serum, as well as many other biological fluids

• Species reactivity- Mammalian

• Applications- The kit provides unique formula and buffers and procedures for detecting the GSH, GSSG, and total glutathione individually.

Features & Benefits:

• Simple procedure; takes only ~1-2 hours

• Fast and convenient

• The assay is easy to perform and detects 2-400 ng/µl of GSH, GSSG or total glutathione.

Kit Components:

• Glutathione Assay Buffer

• PCA (Perchloric Acid, 6N)

• KOH (<6N)

• OPA Probe (o-phthalaldehyde )

• Reducing Agent Mix

• GSH Quencher

• GSH Standard (FW: 307)

Description:

Glutathione is the major intracellular low-molecular-weight thiol that plays a critical role in cellular defense against oxidative stress in tissues and cells. Commercially available glutathione detection kits, such as the DTNB-enzyme cycling glutathione assay kit or the Monochlorobimane based assay kit hardly distinguish between reduced glutathione (GSH; FW: 307) and oxidized glutathione (GSSG; FW: 612). The Glutathione Detection Kit provides a unique, convenient tool for detecting GSH, GSSG, and total glutathione individually. In the assay, OPA, reacts with GSH (not GSSG), generating fluorescence, so GSH can be specifically quantified. Adding a reducing agent converts GSSG to GSH, so (GSH + GSSG) can be determined. To measure GSSG specifically, a GSH Quencher is added to remove GSH, preventing reaction with OPA (while GSSG is unaffected). Reducing agent is then added to destroy excess quencher and to convert GSSG to GSH. Thus, GSSG can be specifically quantified. The kit provides a unique procedure and buffer formula to eliminate protein thiol interference and to stabilize GSH and GSSG in solution.

Storage Conditions: -20°C.

Shipping Conditions: gel pack.

USAGE: For Research Use Only! Not For Use in Humans.

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HansaBioMed Life Sciences提供了从人或动物生物流体，细胞条件培养基和植物提取物中纯化大型（> 150 nm）和小型EV（30-150 nm）的专业知识。可以按照我们的标准方案（结合切向流过滤（TFF）和尺寸排阻色谱（SEC））获得EV净化。或者，可以使用差异超速离心和微滤，化学沉淀或免疫亲和法。

随后，对分离出的电动汽车的总蛋白质含量进行定量，并通过Zetaview（Particle Metrix）进行的纳米颗粒跟踪分析（NTA）进行验证。可根据要求通过ELISA，FACS，TEM，Western印迹进行其他表征。纯化后的电动汽车可以根据需要冻干或冷冻运送给客户。