SAB4200724
Anti-AGO2 antibody, Mouse monoclonal
clone AGO2-10, purified from hybridoma cell culture
동의어(들):
Anti-Argonaute RISC catalytic component 2, Anti-Argonaute2, Anti-Eukaryotic translation initiation factor 2C 2, Anti-PAZ Piwi domain protein (PPD), Anti-Protein Argonaute 2, Anti-eIF2C 2
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모든 사진(2)
About This Item
UNSPSC 코드:
12352203
NACRES:
NA.41
추천 제품
생물학적 소스
mouse
Quality Level
항체 형태
purified from hybridoma cell culture
항체 생산 유형
primary antibodies
클론
AGO2-10, monoclonal
양식
buffered aqueous solution
분자량
~95 kDa
종 반응성
human
농도
~1.0 mg/mL
기술
immunoblotting: 2-4 μg/mL using extract of HEK-293T cells transfected with human AGO2
immunoprecipitation (IP): 10-20 μg/test using HeLa cells extract
동형
IgG1
UniProt 수납 번호
배송 상태
dry ice
저장 온도
−20°C
타겟 번역 후 변형
unmodified
유전자 정보
human ... AGO2(27161)
일반 설명
Anti-AGO2 antibody, Mouse monoclonal (mouse IgG1 isotype) is derived from the AGO2-10 hybridoma produced by the fusion of mouse myeloma cells and splenocytes from a BALB/c mouse immunized with synthetic peptide from the C-terminal region of human AGO2 protein, conjugated to keyhole limpet hemocyanin (KLH). AGO2 is also known as protein argonaute 2, argonaute RNA-induced silencing complex (RISC) catalytic component 2, eukaryotic translation initiation factor 2C 2 (eIF2C2) and PAZ Piwi domain protein (PPD). Argonaute 2 (AGO2) belongs to the Argonaute family. It is located on human chromosome 8q24. Ago proteins localize to the cytoplasm of somatic cells and are concentrated in cytoplasmic processing bodies.
면역원
synthetic peptide from the C-terminal region of human AGO2 protein, conjugated to KLH
애플리케이션
Anti-AGO2 antibody, Mouse monoclonal has been used in immunoblotting and immunoprecipitation.
생화학적/생리학적 작용
Argonaute 2 (AGO2) exhibits intrinsic endonuclease activity. It can directly cleave mRNAs in a small RNA-guided manner. AGO2 plays a central role in RNA silencing processes as essential catalytic components of the RNA-induced silencing complex (RISC). It has an important role in stabilization of circulating microRNAs (miRNAs) in exosomes from extracellular body fluids.
물리적 형태
Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide.
면책조항
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
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Storage Class Code
10 - Combustible liquids
WGK
WGK 1
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
가장 최신 버전 중 하나를 선택하세요:
Lasse Peters et al.
Molecular cell, 26(5), 611-623 (2007-06-15)
Small regulatory RNAs such as short interfering RNAs (siRNAs), microRNAs (miRNAs), and Piwi interacting RNAs (piRNAs) have been discovered in the past, and it is becoming more and more apparent that these small molecules have key regulatory functions. Small RNAs
Andrey Turchinovich et al.
Methods in molecular biology (Clifton, N.J.), 1024, 97-107 (2013-05-31)
Circulating microRNAs (miRNAs) have been recently detected in extracellular body fluids and proved themselves as promising biomarkers for a broad spectrum of diseases. The techniques to isolate, detect, and characterize extracellular miRNAs vary significantly from report to report. In this
Jidong Liu et al.
Science (New York, N.Y.), 305(5689), 1437-1441 (2004-07-31)
Gene silencing through RNA interference (RNAi) is carried out by RISC, the RNA-induced silencing complex. RISC contains two signature components, small interfering RNAs (siRNAs) and Argonaute family proteins. Here, we show that the multiple Argonaute proteins present in mammals are
Argonaute2 promotes tumor metastasis by way of up-regulating focal adhesion kinase expression in hepatocellular carcinoma
Cheng N, et al.
Hepatology, 57(5), 1906-1918 (2013)
Shao-Chun Wu et al.
PloS one, 8(10), e77936-e77936 (2013-11-10)
The levels of circulating microRNAs (miRNAs) in mice with experimental sepsis induced by cecal ligation and puncture (CLP) were determined using whole blood samples obtained from C57BL/6 mice at 4, 8, and 24 h after CLP; miRNA expression analysis was
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