产品详情
产品参数(Product Specifications)
Assay TypeSandwich-ELISAAnalyteAAV8Format96TRegulatory StatusRUOSensitivity<1.75E+07capsids/mLStandard Curve Range5.60E+08 capsids/mL-1.75E+07 capsids/mLAssay Time3 hr 20 minSuitable Sample TypeFor the detection and quantitative determination of AAV8 capsid titration in AAV gene therapy product preparation processing.Sample volume100 uL产品概述(Product Overview)
Adeno-associated virus (AAV) has become one of the most important gene vectors in the field of gene therapy due to its long-term expression, low toxicity, low immunogenicity, and high tissue specificity.Most successful AAV gene therapies for preclinical and clinical studies are limited to natural serotypes, but the presence of neutralizing antibodies against AAV remains a significant barrier to systemic delivery.
应用说明(Application)
AAV8 Titration ELISA Kit was developed for the detection and quantitative determination of AAV8 capsid titration in AAV gene therapy product preparation processing.
It is for research use only.
重构方法(Reconstitution)
Please see Certificate of Analysis for details of reconstitution instruction and specific concentration.
存储(Storage)
2-8℃
组分(Materials Provided)
IDComponentsSizeAAV08-C01Pre-coated Anti-AAV8 Antibody Microplate1 plateAAV08-C02AAV8 Standard1.4E+10 capsidsAAV08-C03Biotin-Anti-AAV8 Antibody15 μgAAV08-C04Streptavidin-HRP50 μLAAV08-C0510×Washing Buffer50 mLAAV08-C062×Dilution Buffer50 mLAAV08-C07Substrate Solution12 mLAAV08-C08Stop Solution7 mL原理(Assay Principles)
This assay kit employs a standard sandwich-ELISA format, providing a rapid detection of AAV8 capsid. The kit consists of Pre-coated Anti-AAV8 Antibody Microplate and AAV8 Standard, Biotin-Anti-AAV8 Antibody, Streptavidin-HRP and buffers.
Your experiment will include 6 simple steps:
a) Bring all reagents to room temperature(20℃-25℃) before use.
b) Add your sample to the plate and take the AAV8 capsid as standard. The samples and standard are diluted by Dilution Buffer.
c) Wash the plate and add the Biotin-Anti-AAV8 Antibody diluted by Dilution Buffer to the plate.
e) Wash the plate and add TMB.
f) Stop the substrate reaction by adding diluted acid. Absorbance (OD) is calculated by the absorbance at 450 nm minus the absorbance at 630 nm to remove background disturbance before statistical analysis. The OD Value reflects the amount of bound protein.
质量管理控制体系(QMS)
产品展示
典型数据-Typical Data
Please refer to DS document for the assay protocol.
For each experiment, a standard curve needs to be set for each micro-plate, and the specific OD value may vary depending on different laboratories, testers, or equipments. The following example data is for reference only.
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