SNRPN Rabbit Polyclonal Antibody

CAT#: TA362799

SNRPN Antibody - middle region



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CNY 5,250.00


货期*
6周

规格
    • 50 ug

Product images

经常一起买 (3)
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Recombinant protein of human small nuclear ribonucleoprotein polypeptide N (SNRPN), transcript variant 2, 20 µg
    • 20 ug

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Transient overexpression lysate of small nuclear ribonucleoprotein polypeptide N (SNRPN), transcript variant 1
    • 100 ug

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Specifications

Product Data
Applications WB
Reactivity Human
Host Rabbit
Clonality Polyclonal
Immunogen The immunogen is a synthetic peptide directed towards the middle region of human SNRPN
Specificity Expected reactivity: Human
Formulation Liquid. Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
Note that this product is shipped as lyophilized powder to China customers.
Concentration lot specific
Purification Affinity purified
Conjugation Unconjugated
Storage Condition For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
Predicted Protein Size 26 kDa
Gene Name small nuclear ribonucleoprotein polypeptide N
Background This gene is located within the Prader-Willi Syndrome critical region on chromosome 15 and is imprinted and expressed from the paternal allele. It encodes a component of the small nuclear ribonucleoprotein complex, which functions in pre-mRNA processing and may contribute to tissue-specific alternative splicing. Alternative promoter use and alternative splicing result in a multitude of transcript variants encoding the same protein. Transcript variants that initiate at the CpG island-associated imprinting center may be bicistronic and also encode the SNRPN upstream reading frame protein (SNURF) from an upstream open reading frame. In addition, long spliced transcripts for small nucleolar RNA host gene 14 (SNHG14) may originate from the promoters at this locus and share exons with this gene. Alterations in this region are associated with parental imprint switch failure, which may cause Angelman syndrome or Prader-Willi syndrome.
Synonyms DKFZp686C0927; DKFZp686M12165; DKFZp761I1912; DKFZp762N022; FLJ33569; FLJ36996; FLJ39265; HCERN3; MGC29886; PWCR; RT-LI; SM-D; Sm-N; SMN; SNRNP-N; SNURF-SNRPN
Reference Data
Protein Families Stem cell - Pluripotency
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.
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