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PSPC1 Polyclonal Antibody Reactivity Human

SKU: E-AB-52739-200

  • $ 55995
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PSPC1 Polyclonal Antibody Reactivity Human

 

SKU # E-AB-52739
Reactivity Human, Mouse, Rat
Host Rabbit
Applications IHC

 

Product Details

Isotype IgG
Host Rabbit
Reactivity Human, Mouse, Rat
Applications IHC
Clonality Polyclonal
Immunogen Fusion protein of human PSPC1
Abbre PSPC1
Synonyms PSP1,  PSPC1,  Paraspeckle component 1,  Paraspeckle protein 1,  Pspc1
Swissprot
Cellular Localization Nucleus>nucleolus. Nucleus matrix. Cytoplasm. In punctate subnuclear structures often located adjacent to splicing speckles, called paraspeckles. Colocalizes with NONO and SFPQ in paraspeckles and perinucleolar caps in a RNA-dependent manner. May cycles between paraspeckles and nucleolus. In telophase, when daughter nuclei form, localizes to perinucleolar caps.
Concentration 0.48 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
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
IHC 1:30-1:150

 

Background

This gene encodes a nucleolar protein that localizes to punctate subnuclear structures that occur close to splicing speckles, known as paraspeckles.These paraspeckles are composed of RNA-protein structures that include a non-coding RNA, NEAT1/Men epsilon/beta, and the Drosophila Behavior Human Splicing family of proteins, which include the product of this gene and the P54NRB/NONO and PSF/SFPQ proteins.Paraspeckles may function in the control of gene expression via an RNA nuclear retention mechanism.The protein encoded by this gene is found in paraspeckles in transcriptionally active cells, but it localizes to unique cap structures at the nucleolar periphery when RNA polymerase II transcription is inhibited, or during telophase.Alternative splicing of this gene results in multiple transcript variants.A related pseudogene, which is also located on chromosome 13, has been identified.