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EWSR1 Polyclonal Antibody Reactivity Human

SKU: E-AB-52908-200

  • $ 55995
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EWSR1 Polyclonal Antibody Reactivity Human

 

SKU # E-AB-52908
Reactivity Human, Mouse
Host Rabbit
Applications IHC

 

Product Details

Isotype IgG
Host Rabbit
Reactivity Human, Mouse
Applications WB, IHC
Clonality Polyclonal
Immunogen Fusion protein of human EWSR1
Abbre EWSR1
Synonyms EWS,  EWS RNA binding protein 1,  EWS oncogene,  EWSR 1,  EWSR1 protein,  Ewing sarcoma breakpoint region 1,  Ewing sarcoma breakpoint region 1 protein,  Ewings sarcoma EWS Fli1 type 1 oncogene,  Ewsr1,  RNA,  bK984G1.4,  bK984G1.4 Ewing sarcoma breakpoint region 1 protein
Swissprot
Calculated MW 68 kDa
Observed MW Refer to figures
Cellular Localization Nucleus. Cytoplasm. Cell membrane. Relocates from cytoplasm to ribosomes upon PTK2B/FAK2 activation.
Concentration 1.08 mg/mL
Buffer Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol.
Purification Method Antigen affinity purification
Research Areas Cancer,  Epigenetics and Nuclear Signaling,  Tags and Cell Markers
Conjugation Unconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Shipping The product is shipped with ice pack, upon receipt, store it immediately at the temperature recommended.

 

Related Reagents

Applications Recommended Dilution
WB 1:1000-1:5000
IHC 1:50-1:300

 

Background

This gene encodes a multifunctional protein that is involved in various cellular processes, including gene expression, cell signaling, and RNA processing and transport. The protein includes an N-terminal transcriptional activation domain and a C-terminal RNA-binding domain. Chromosomal translocations between this gene and various genes encoding transcription factors result in the production of chimeric proteins that are involved in tumorigenesis. These chimeric proteins usually consist of the N-terminal transcriptional activation domain of this protein fused to the C-terminal DNA-binding domain of the transcription factor protein. Mutations in this gene, specifically a t(11;22)(q24;q12) translocation, are known to cause Ewing sarcoma as well as neuroectodermal and various other tumors. Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 1 and 14.