Saltar al contenido
Merck

SAB4200454

Sigma-Aldrich

Anti-FUS antibody produced in rabbit

enhanced validation

~1.0 mg/mL, affinity isolated antibody

Sinónimos:

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

Iniciar sesiónpara Ver la Fijación de precios por contrato y de la organización


About This Item

Código UNSPSC:
12352203
NACRES:
NA.41

origen biológico

rabbit

Nivel de calidad

conjugado

unconjugated

forma del anticuerpo

affinity isolated antibody

tipo de anticuerpo

primary antibodies

clon

polyclonal

formulario

buffered aqueous solution

mol peso

antigen ~68 kDa

reactividad de especies

rat, human

validación mejorada

independent
Learn more about Antibody Enhanced Validation

concentración

~1.0 mg/mL

técnicas

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.

Nº de acceso UniProt

Condiciones de envío

dry ice

temp. de almacenamiento

−20°C

modificación del objetivo postraduccional

unmodified

Información sobre el gen

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

Descripción general

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.

Especificidad

Anti-FUS specifically recognizes human and rat FUS.

Inmunógeno

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.

Aplicación

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

Acciones bioquímicas o fisiológicas

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.

Forma física

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

Almacenamiento y estabilidad

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.

Cláusula de descargo de responsabilidad

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.

¿No encuentra el producto adecuado?  

Pruebe nuestro Herramienta de selección de productos.

Código de clase de almacenamiento

10 - Combustible liquids

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

¿Ya tiene este producto?

Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.

Visite la Librería de documentos

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)
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
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)
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

Nuestro equipo de científicos tiene experiencia en todas las áreas de investigación: Ciencias de la vida, Ciencia de los materiales, Síntesis química, Cromatografía, Analítica y muchas otras.

Póngase en contacto con el Servicio técnico