老带新
FastScan AsCpf1/Cas12a (Strain BV3L6 ) ELISA Kit

FastScan AsCpf1/Cas12a (Strain BV3L6 ) ELISA Kit

分享
品牌: CST
用小程序,查商品更便捷
收藏
对比对比
咨询咨询
产品介绍
产品介绍
产品信息
简单描述

The FastScan™ AsCpf1/Cas12a (Strain BV3L6) ELISA Kit is a sandwich enzyme-linked immunosorbent assay (ELISA) that detects AsCpf1/Cas12a (Strain BV3L6). To perform the assay, sample is incubated with a capture antibody conjugated with a proprietary tag and a second detection antibody linked to HRP, forming a sandwich with AsCpf1/Cas12a (Strain BV3L6) in solution. This entire complex is immobilized to the plate via an anti-tag antibody. The wells are then washed to remove unbound material. TMB is then added. The magnitude of observed signal is proportional to the quantity of AsCpf1/Cas12a (Strain BV3L6).

*Antibodies in kit are custom formulations specific to kit.

IMPORTANT: This FastScan™ ELISA Kit requires 4 washes at Step 6 of the protocol.

应用
目标/特异性

Specificity/Sensitivity

The FastScan™ AsCpf1/Cas12a (Strain ) ELISA Kit detects AsCpf1/Cas12a (Strain ), as shown in Figure 1. This kit detects proteins from the indicated species, as determined through in-house testing, but may also detect homologous proteins from other species.

Species Reactivity:

All Species Expected

背景
背景
CRISPR-Cas (clustered regularly interspaced short palindromic repeats and CRISPR-associated proteins) are RNA-guided nuclease effectors that are utilized for precise genome editing in mammalian systems (1). Cpf1/Cas12a (CRISPR from Prevotella and Francisella) proteins are members of the Class 2 CRISPR system (2). Class 2 CRISPR systems, such as the well characterized Cas9, rely on single-component effector proteins to mediate DNA interference (3). Cpf1/Cas12a endonucleases, compared to Cas9 systems, have several unique features that increase the utility of CRISPR-based genome editing techniques: 1) Cpf1/Cas12a-mediated cleavage relies on a single and short CRISPR RNA (crRNA) without the requirement of a trans-activating crRNA (tracrRNA), 2) Cpf1/Cas12a utilizes T-Rich protospacer-adjacent motif (PAM) sequences rather than a G-Rich PAM, and 3) Cpf1/Cas12a generates a staggered, rather than a blunt-ended, DNA double-stranded break (2). These features broaden the utility of using CRISPR-Cas systems for specific gene regulation and therapeutic applications. Several Cpf1/Cas12a bacterial orthologs have been characterized for CRISPR-mediated mammalian genome editing (2,4).AsCpf1/Cas12a (Strain BV3L6) is a Cpf1/Cas12a enzyme derived from Acidaminococcus sp. BV3L6 (5,6). 1.Cong, L. et al. (2013) Science 339, 819-23. 2.Zetsche, B. et al. (2015) Cell 163, 759-71. 3.Horvath, P. and Barrangou, R. (2010) Science 327, 167-70. 4.Zhang, Y. et al. (2017) Sci Adv 3, e1602814. 5.Zetsche, B. et al. (2015) Cell 163, 759-71. 6.Zhang, Y. et al. (2017) Sci Adv 3, e1602814.
翻译后修饰
unmodified
数据库链接
UniProt ID
U2UMQ6
声明 :本官网所有报价均为常温或者蓝冰运输价格,如有产品需要干冰运输,需另外加收干冰运输费。
货号:
58693C
一键复制
询价
1 Kit
5 Kit
10 Kit
20 Kit
50 Kit
选择数量
当前规格1件起购 
配送至
预计2-3周送达,快递: 免运费,若需干冰额外收费