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SAB4200478

Sigma-Aldrich

Monoclonal Anti-FUS antibody produced in mouse

clone FUS-4, tissue culture supernatant

同義詞:

Monoclonal Anti-75 kDa DNA-pairing protein, Monoclonal Anti-ALS6, Monoclonal Anti-FUS1, Monoclonal Anti-HNRNPP2, Monoclonal Anti-POMP75, Monoclonal Anti-TLS, Monoclonal Anti-fused in sarcoma, Monoclonal Anti-fusion gene in myxoid liposarcoma, Monoclonal Anti-heterogeneous nuclear ribonucleoprotein P2, Monoclonal Anti-translocated in liposarcoma protein

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About This Item

分類程式碼代碼:
12352203
NACRES:
NA.41

生物源

mouse

品質等級

共軛

unconjugated

抗體表格

tissue culture supernatant

抗體產品種類

primary antibodies

無性繁殖

FUS-4, monoclonal

形狀

buffered aqueous solution

分子量

antigen ~70 kDa

物種活性

mouse, human, rat

技術

immunohistochemistry: 1:500-1:1000 using formalin-fixed and paraffin embedded rat cerebellum.
indirect immunofluorescence: 1:200-1:400 using using HeLa or HepG2 cells.
western blot: 1:1000-1:2000 using lysates of G361 cells.

同型

IgM

UniProt登錄號

運輸包裝

dry ice

儲存溫度

−20°C

目標翻譯後修改

unmodified

基因資訊

human ... FUS(2521)
mouse ... Fus(233908)
rat ... Fus(317385)

一般說明

Monoclonal Anti-FUS (mouse IgM isotype) is derived from the hybridoma FUS-4 produced by the fusion of mouse myeloma cells and splenocytes from BALB/c mice immunized with a synthetic peptide corresponding to an internal sequence of human FUS, conjugated to KLH. Fused in sarcoma (FUS), also known as translocated in liposarcoma (TLS), ribonucleoprotein (RNP)-P2, amyotrophic lateral sclerosis-6 (ALS6), is a RNA/DNA binding protein. FUS is normally located predominantly in the nucleus whereas, pathological FUS inclusions are mostly found in the cytosol of neurons and glia cells.

免疫原

synthetic peptide corresponding to an internal sequence of human FUS, conjugated to KLH. The corresponding sequence is identical in monkey and differs by 3 amino acids in mouse and rat.

應用

Monoclonal Anti-FUS antibody produced in mouse has been used in various immunochemical techniques including:
  • immunoblotting
  • immunofluorescence
  • immunohistochemistry

生化/生理作用

Fused in sarcoma (FUS) plays a vital role in transcription, RNA splicing and transport and is implicated in multiple diseases. Mutations in TAR DNA binding protein 43 (TDP-43) and FUS is associated with the development of amyotrophic lateral sclerosis (ALS) and fronto-temporal lobar degeneration (FLTD) including ubiquitin-positive inclusions (FLTDU). The majority of the FUS mutations has been recognized in C-terminal nuclear localization signal (NLS). FUS has been implicated in a broadening spectrum of neurodegenerative disorders. FUS has been identified as a component of inclusion bodies in patients with Huntington′s disease (HD) and spinocerebellar ataxias (SCA1-3).

外觀

Culture supernatant solution containing 15 mM sodium azide.

免責聲明

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.

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儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 2

閃點(°F)

Not applicable

閃點(°C)

Not applicable


分析證明 (COA)

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存取文件庫

ALS/FTD-linked mutation in FUS suppresses intra-axonal protein synthesis and drives disease without nuclear loss-of-function of FUS
Lopez-Erauskin J, et al.
Neuron, 100(4), 816-830 (2018)
TDP-43 and FUS/TLS: emerging roles in RNA processing and neurodegeneration
Lagier-Tourenne C, et al.
Human Molecular Genetics, 19(R1), R46-R64 (2010)
TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia
Mackenzie IRA, et al.
Lancet Neurology, 9(10), 995-1007 (2010)
Gain of Additional BIRC3 Protein Functions through xn-3-t6a-UTR-Mediated Protein Complex Formation
Lee SH and Mayr C
Molecular Cell, 74(4), 701-712 (2019)
A Membraneless Organelle Associated with the Endoplasmic Reticulum Enables 3'UTR-Mediated Protein-Protein Interactions
Ma W and Mayr C
Cell, 175(6), 1492-1506 (2018)

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