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Merck
모든 사진(2)

Key Documents

SAB4200511

Sigma-Aldrich

Anti-FUS (internal region) antibody produced in rabbit

affinity isolated antibody

동의어(들):

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

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About This Item

UNSPSC 코드:
12352203
NACRES:
NA.41

생물학적 소스

rabbit

Quality Level

결합

unconjugated

항체 형태

affinity isolated antibody

항체 생산 유형

primary antibodies

클론

polyclonal

형태

buffered aqueous solution

분자량

antigen ~70 kDa

종 반응성

human

기술

indirect immunofluorescence: 2.5-5.0 μg/mL using human HepG2 or MCF7 cells.
western blot: 0.5-1.0 μg/mL using whole extracts of human HEK-293T or G361 cells.

UniProt 수납 번호

배송 상태

dry ice

저장 온도

−20°C

타겟 번역 후 변형

unmodified

유전자 정보

human ... FUS(2521)

일반 설명

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

특이성

Anti-FUS (internal region) recognizes human FUS.

면역원

peptide corresponding to an internal region of human FUS, conjugated to KLH. The corresponding sequence is identical in monkey and differs by 4 amino acids in rat and mouse.

애플리케이션

Anti-FUS (internal region) antibody produced in rabbit may be used in:
  • immunoblotting
  • immunofluorescence
  • immunohistochemistry

생화학적/생리학적 작용

Fused in sarcoma (FUS), also called translocation in liposarcoma or Tumor lysis syndrome (TLS), plays a key role in RNA splicing, DNA repair and transcriptional regulation. It is a RNA/DNA binding protein implicated in various diseases. Mutations in the FUS gene is implicated in familial amyotrophic lateral sclerosis (FALS). Chromosomal translocation of FUS/TLS is found in human cancers and results in the production of oncogenic FUS fusion proteins. FUS has been implicated in a broadening spectrum of neurodegenerative disorders and is a component of inclusion bodies in patients with Huntington′s disease (HD) and spinocerebellar ataxias (SCA1) and SCA3. The majority of the FUS mutations have been identified in the C-terminal nuclear localization signal (NLS). TAR DNA-binding protein 43 (TDP-43) and FUS have been identified in amyotrophic lateral sclerosis (ALS), frontotemporal lobar degeneration (FLTD) and familial amyotrophic lateral sclerosis (FALS). Pathological FUS inclusions are mostly found in the cytosol of neurons and glial cells.

물리적 형태

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

저장 및 안정성

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

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

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


시험 성적서(COA)

제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.

이 제품을 이미 가지고 계십니까?

문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

TDP-43 and FUS: a nuclear affair
Dormann D and Haass C
Trends in Neurosciences, 34(7), 339-348 (2011)
Fused in sarcoma: Properties, self-assembly and correlation with neurodegenerative diseases
Chen C, et al.
Molecules (Basel), 24(8), 1622-1622 (2019)
Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation
Chio A, et al.
Neurobiology of Aging, 30(8), 1272-1275 (2009)
Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6
Vance C, et al.
Science (New York, N.Y.), 323(5918), 1208-1211 (2009)
Hao Deng et al.
Nature reviews. Neurology, 10(6), 337-348 (2014-05-21)
The neurodegenerative diseases are a diverse group of disorders characterized by progressive loss of specific groups of neurons. These diseases affect different populations, and have a variable age of onset, clinical symptoms, and pathological findings. Variants in the FUS gene

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