验证数据展示
经过测试的应用
Positive FC (Intra) detected in | Transfected Vero |
推荐稀释比
应用 | 推荐稀释比 |
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Flow Cytometry (FC) (INTRA) | FC (INTRA) : 0.4 ug per 10^6 cells in a 100 µl suspension |
It is recommended that this reagent should be titrated in each testing system to obtain optimal results. | |
Sample-dependent, Check data in validation data gallery. |
产品信息
CL488-85780-2 targets dsRNA in FC (Intra), ELISA applications and shows reactivity with n/a samples.
经测试应用 | FC (Intra), ELISA Application Description |
经测试反应性 | n/a |
免疫原 | Peptide 种属同源性预测 |
宿主/亚型 | Rabbit / IgG |
抗体类别 | Recombinant |
产品类型 | Antibody |
全称 | dsRNA |
别名 | 250708A2 |
基因名称 | |
Gene ID (NCBI) | |
偶联类型 | CoraLite®488 Fluorescent Dye |
最大激发/发射波长 | 491 nm / 516 nm |
形式 | Liquid |
纯化方式 | Protein A purification |
储存缓冲液 | PBS with 50% glycerol, 0.05% Proclin300, 0.5% BSA, pH 7.3. |
储存条件 | Store at -20°C. Avoid exposure to light. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. |
背景介绍
dsRNA is formed by the base pairing of two RNA strands, creating a double helix structure similar to DNA, but with some differences. dsRNA can be generated through various mechanisms. In the context of viral infections, it can be derived from the genomes of dsRNA viruses, replication intermediates of single-stranded RNA viruses, or bidirectional transcription of certain DNA viruses. Additionally, aberrant splicing or transcriptional processes may lead to the formation of dsRNA structures. dsRNA is recognized as a pathogen-associated molecular pattern (PAMP) by the immune system. It can trigger a series of immune responses in cells, including the activation of antiviral innate immune pathways.
实验方案
Product Specific Protocols | |
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FC protocol for CL488 dsRNA antibody CL488-85780-2 | Download protocol |
Standard Protocols | |
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Click here to view our Standard Protocols |