Huntingtin Associated Protein 1 (HAP1) (NM_001079871) Human Tagged ORF Clone Lentiviral Particle

SKU RC220440L1V

Lenti ORF particles, HAP1 (Myc-DDK tagged) - Human huntingtin-associated protein 1 (HAP1), transcript variant 4, 200ul, >10^7 TU/mL

Product Data

• Type: Human Tagged ORF Clone Lentiviral Particle
• Tag: Myc-DDK
• Target Symbol: Huntingtin Associated Protein 1
• Synonyms: HAP2; hHLP1; HIP5; HLP
• Vector: pLenti-C-Myc-DDK
• Mammalian Cell Selection: None
• Sequence Data:
  ORF Nucleotide Sequence

  The ORF insert of this clone is exactly the same as(RC220440).
• ACCN: NM_001079871
• ORF Size: 1782 bp
• OTI Disclaimer: The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info
• OTI Annotation: This clone was engineered to express the complete ORF with an expression tag. Expression varies depending on the nature of the gene.
• Shipping: Dry Ice

Reference Data

• RefSeq: NM_001079871.1, NP_001073340.1
• RefSeq Size: 3869 bp
• RefSeq ORF: 1785 bp
• Locus ID: 9001
• UniProt ID: P54257
• Cytogenetics: 17q21.2
• Protein Pathways: Huntington's disease
• MW: 66.5 kDa
• Summary: Huntington's disease (HD), a neurodegenerative disorder characterized by loss of striatal neurons, is caused by an expansion of a polyglutamine tract in the HD protein huntingtin. This gene encodes a protein that interacts with huntingtin, with two cytoskeletal proteins (dynactin and pericentriolar autoantigen protein 1), and with a hepatocyte growth factor-regulated tyrosine kinase substrate. The interactions with cytoskeletal proteins and a kinase substrate suggest a role for this protein in vesicular trafficking or organelle transport. Several alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]