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Merck
CN

SAB4200454

Sigma-Aldrich

Anti-FUS antibody produced in rabbit

enhanced validation

~1.0 mg/mL, affinity isolated antibody

别名:

Anti-ALS6, Anti-CHOP, Anti-FUS-CHOP, Anti-FUS1, Anti-TLS, Anti-TLS/CHOP, Anti-hnRNP-P2

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About This Item

UNSPSC代码:
12352203
NACRES:
NA.41

生物来源

rabbit

质量水平

偶联物

unconjugated

抗体形式

affinity isolated antibody

抗体产品类型

primary antibodies

克隆

polyclonal

形式

buffered aqueous solution

分子量

antigen ~68 kDa

种属反应性

rat, human

增强验证

independent
Learn more about Antibody Enhanced Validation

浓度

~1.0 mg/mL

技术

immunohistochemistry: 5-10 μg/mL using formalin-fixed paraffin embedded rat colon.
indirect immunofluorescence: 2.5-5 μg/mL using HeLa cells.
western blot: 1.5-3.0 μg/mL using using lysates of Jurkat cells.

UniProt登记号

运输

dry ice

储存温度

−20°C

靶向翻译后修饰

unmodified

基因信息

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

相关类别

一般描述

Fused in sarcoma (FUS) is a component of heterogeneous nuclear ribonucleoprotein (hnRNP) complex is a DNA/ RNA binding protein. FUS gene is mapped to human chromosome 16p11.2 and is located predominantly in the nucleus.

特异性

Anti-FUS specifically recognizes human and rat FUS.

免疫原

synthetic peptide corresponding to the N-terminal region of human FUS isoform 1, conjugated to KLH. The corresponding sequence is identical in human FUS isoforms 2 and 3, and highly conserved (single amino acid insertion) in mouse and rat FUS.

应用

Anti-FUS antibody produced in rabbit has been used in:
  • immunohistochemistry
  • immunoblotting
  • immunofluorescence

生化/生理作用

Fused in sarcoma (FUS) plays regulatory roles in transcription, RNA splicing and transport and is implicated in multiple diseases. FUS also called translocation in liposarcoma or Tumor lysis syndrome (TLS), plays a key role in DNA repair and transcriptional regulation. Chromosomal translocation of FUS/TLS is found in human cancers and results in the production of oncogenic FUS fusion proteins. FUS is a component of inclusion bodies in patients with Huntington′s disease (HD) and spinocerebellar ataxias (SCA1) and SCA3. Mutations in the FUS gene have been identified in amyotrophic lateral sclerosis (ALS), frontotemporal lobar degeneration (FLTD) and familial amyotrophic lateral sclerosis (FALS). The majority of the FUS mutations have been identified in the C-terminal nuclear localization signal (NLS). Pathological FUS inclusions are mostly found in the cytosol of neurons and glial cells.

外形

Solution in 0.01 M phos­phate buffered saline, pH 7.4, containing 15 mM sodium azide.

储存及稳定性

For continuous use, store at 2-8 °C for up to one month. For extended storage, freeze in working aliquots. Repeated freezing and thawing, or storage in “frost-free” freezers,is not recommended. If slight turbidity occurs upon prolonged storage, clarify the solution by centrifugation before use. Working dilutions should be discarded if not used within 12 hours.

免责声明

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.

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闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

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Tomas Smolek et al.
The Journal of comparative neurology, 524(4), 874-895 (2015-08-05)
Canine cognitive impairment syndrome (CDS) represents a group of symptoms related to the aging of the canine brain. These changes ultimately lead to a decline of memory function and learning abilities, alteration of social interaction, impairment of normal housetraining, and
Atypical Huntington?s disease with the clinical presentation of behavioural variant of frontotemporal dementia
Sutovsky S, et al.
Journal of neural transmission (Vienna, Austria : 1996), 123(12), 1423-1433 (2016)
Tau hyperphosphorylation in synaptosomes and neuroinflammation are associated with canine cognitive impairment
Smolek T, et al.
The Journal of Comparative Neurology, 524(4), 874-895 (2016)
Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation
Chio A, et al.
Neurobiology of Aging, 30(8), 1272-1275 (2009)
Fused in sarcoma: Properties, self-assembly and correlation with neurodegenerative diseases
Chen C, et al.
Molecules (Basel), 24(8), 1622-1622 (2019)

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