- 当前位置:首页 > >Merck Millipore > 生命科学研究
- 生命科学研究
-

-
merck millipore,默克密理博,04-1552,Anti-TLS Antibody, clone 1FU-1D2
产品名称:Anti-TLS Antibody, clone 1FU-1D2
产品型号:04-1552
Use Anti-TLS Antibody, clone 1FU-1D2 (Mouse Monoclonal Antibody) validated in WB, ICC to detect TLS also known as 75 kDa DNA-pairing protein, FUS-CHOP fusion protein.
merck millipore,默克密理博,04-1552,Anti-TLS Antibody, clone 1FU-1D2
- 产品介绍
重要规格表
品种反应性 主要应用 宿主 格式 抗体类型 R, H, M ICC, WB M Ascites Monoclonal Antibody 描述 产品目录编号 04-1552 描述 Anti-TLS Antibody, clone 1FU-1D2 Alternate Names - translocated in liposarcoma
- 75 kDa DNA-pairing protein
- FUS-CHOP fusion protein
- FUS-CHOP protein fusion
- Fusion gene in myxoid liposarcoma
- Oncogene FUS
- Oncogene TLS
- Translocated in liposarcoma protein
- fus-like protein
- fus/tls-chop oncogene
- fusion (involved in t(12
- 16) in malignant liposarcoma)
- fusion, derived from t(12
- 16) malignant liposarcoma
- heterogeneous nuclear ribonucleoprotein P2
背景信息 The TLS/FUS protein contains an RNA-recognition motif and is a component of nuclear riboprotein complexes. It resembles a transcription factor in that it binds DNA, contributes a transcriptional activation domain to the FUS-ERG oncoprotein, and interacts with several transcription factors in vitro. It binds both single-stranded and double-stranded DNA and promotes ATP-independent annealing of complementary single-stranded DNAs and D-loop formation in superhelical double-stranded DNA. It may play a role in maintenance of genomic integrity. 产品信息 格式 Ascites 控制 - HepG2 cell lysate
演示 Unpurified mouse monoclonal IgG1κ preservative-free ascites. 应用 应用 Use Anti-TLS Antibody, clone 1FU-1D2 (Mouse Monoclonal Antibody) validated in WB, ICC to detect TLS also known as 75 kDa DNA-pairing protein, FUS-CHOP fusion protein. 主要应用 - Immunocytochemistry
- Western Blotting
应用说明 Immunocytochemistry Analysis:
1:500 dilution from a representative lot detected TLS in C2C12 cells.生物信息 免疫原品种 Linear peptide corresponding to human TLS. 表位 Unknown 克隆 clone 1FU-1D2 宿主 Mouse 特异性 This antibody recognizes TLS. 同种型 IgG1κ 品种反应性 RatHumanMouse Species Reactivity Note Demonstrated to react with human, mouse, and rat. 抗体类型 Monoclonal Antibody Entrez基因编号 - NP_004951.1
Entrez基因汇总 This gene encodes a multifunctional protein component of the heterogeneous nuclear ribonucleoprotein (hnRNP) complex. The hnRNP complex is involved in pre-mRNA splicing and the export of fully processed mRNA to the cytoplasm. This protein belongs to the FET family of RNA-binding proteins which have been implicated in cellular processes that include regulation of gene expression, maintenance of genomic integrity and mRNA/microRNA processing. Alternative splicing results in multiple transcript variants. Defects in this gene result in amyotrophic lateral sclerosis type 6. [provided by RefSeq]. 基因符号 - hnRNP-P2
- FUS
- CHOP
- FUS-CHOP
- FUS1
- POMp75
- TLS
- TLS/CHOP
纯化方法 Unpurified UniProt编号 - P35637
UniProt汇总 FUNCTION: Binds both single-stranded and double-stranded DNA and promotes ATP-independent annealing of complementary single-stranded DNAs and D-loop formation in superhelical double-stranded DNA. May play a role in maintenance of genomic integrity.
SUBUNIT STRUCTURE: Component of nuclear riboprotein complexes. Interacts with ILF3, TDRD3 and SF1. Interacts through its C-terminus with SFRS13A. Interacts with OTUB1 and SARNP.
SUBCELLULAR LOCATION: Nucleus
TISSUE SPECIFICITY: Ubiquitous.
PTM: Arg-216 and Arg-218 are dimethylated, probably to asymmetric dimethylarginine.
INVOLVEMENT IN DISEASE: A chromosomal aberration involving FUS is a cause of a form of malignant myxoid liposarcoma. Translocation t(12;16)(q13;p11) with DDIT3.
A chromosomal aberration involving FUS is a cause of acute myeloid leukemia (AML). Translocation t(16;21)(p11;q22) with ERG.
A chromosomal aberration involving FUS is associated with angiomatoid fibrous histiocytoma (AFH) [MIM:612160]. Translocation t(12;16)(q13;p11.2) with ATF1 generates a chimeric FUS/ATF1 protein.
Defects in FUS are the cause of amyotrophic lateral sclerosis type 6 (ALS6) [MIM:608030]. ALS6 is a familial form of amyotrophic lateral sclerosis. ALS is a neurodegenerative disorder affecting upper motor neurons in the brain and lower motor neurons in the brain stem and spinal cord, resulting in fatal paralysis. Sensory abnormalities are absent. Death usually occurs within 2 to 5 years. The etiology of amyotrophic lateral sclerosis is likely to be multifactorial, involving both genetic and environmental factors. The disease is inherited in 5-10%.
SEQUENCE SIMILARITIES: Belongs to the RRM TET family.
Contains 1 RanBP2-type zinc finger.
Contains 1 RRM (RNA recognition motif) domain.产品使用声明 质量保证 Evaluated by Western Blot in HepG2 cell lysate.
Western Blot Analysis: 1:1,000 dilution of this antibody detected TLS on 10 µg of HepG2 cell lysate.使用声明 - 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.
储存和货运信息 存储条件 Stable for 1 year at -20°C from date of receipt.
Handling Recommendations: Upon receipt and prior to removing the cap, centrifuge the vial and gently mix the solution. Aliquot into microcentrifuge tubes and store at -20°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance.包装信息 数量 100 µL
上一件merck millipore产品:merck millipore,默克密理博,AB6017,Anti-F-actin-capping protein subunit beta Antibody
下一件merck millipore产品:merck millipore,默克密理博,AG502,Human IgG1 kappa
merck millipore,默克密理博,04-1003,Anti-acetyl-Histone H3 (Lys9) Antibody, clone Y28, rabbit monoclonal
merck millipore,默克密理博,FCABS419PE,Milli-Mark™ Anti-PRMT5-PE Antibody
merck millipore,默克密理博,ABN272,Anti-GPRASP1 Antibody
merck millipore,默克密理博,203988,Butyrolactone I - CAS 87414-49-1 - Calbiochem
merck millipore,默克密理博,AB6017,Anti-F-actin-capping protein subunit beta Antibody
merck millipore,默克密理博,AG502,Human IgG1 kappa
merck millipore,默克密理博,ABC144,Anti-Syntaxin 8 Antibody
merck millipore,默克密理博,14-329,JNK2α2/SAPK1a Protein, active, 10 µg
merck millipore,默克密理博,MAB3908,Anti-Na+/H+ Exchanger Isoform NHE8 Antibody
merck millipore,默克密理博,07-1347,Anti-phospho-STAT3 (Tyr68) Antibody


