Human SNRPN activation kit by CRISPRa

CAT#: GA104550

SNRPN CRISPRa kit - CRISPR gene activation of human small nuclear ribonucleoprotein polypeptide N

Product Images

Specifications

Product Data

• Format: 3gRNAs, 1 scramble ctrl and 1 enhancer vector
• Symbol: SNRPN
• Locus ID: 6638
• Kit Components:

  GA104550G1, SNRPN gRNA vector 1 in pCas-Guide-GFP-CRISPRa

  GA104550G2, SNRPN gRNA vector 2 in pCas-Guide-GFP-CRISPRa

  GA104550G3, SNRPN gRNA vector 3 in pCas-Guide-GFP-CRISPRa

  1 CRISPRa-Enhancer vector, SKU GE100056

  1 CRISPRa scramble vector, SKU GE100077

• Disclaimer: The kit is designed based on the best knowledge of CRISPa SAM technology. The efficiency of the activation can be affected by many factors, including nucleosome occupancy status, chromatin structure and the gene expression level of the target, etc.

Reference Data

• RefSeq: NM_003097, NM_022805, NM_022806, NM_022807, NM_022808, NM_001349454, NM_001349455, NM_001349456, NM_001349457, NM_001349458, NM_001349459, NM_001349460, NM_001349461, NM_001349462, NM_001349463, NM_001349464, NM_001349465
• Synonyms: HCERN3; PWCR; PWS; RT-LI; SM-D; sm-N; SMN; SNRNP-N; SNURF-SNRPN
• Summary: '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. [provided by RefSeq, Mar 2017]'