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SR317358

KRTAP8-1 Human siRNA Oligo Duplex (Locus ID 337879)

Origene Technologies, Inc.

DESCRIPTION

KRTAP8-1 (Human) - 3 unique 27mer siRNA duplexes - 2 nmol each

DETAILS

  • Note: Single siRNA duplex (10nmol) can be ordered.
  • Purity: HPLC purified
  • Refseq: NM_175857
  • Status: 3 Weeks*
  • Summary: In the hair cortex, hair keratin intermediate filaments are embedded in an interfilamentous matrix, consisting of hair keratin-associated proteins (KRTAP), which are essential for the formation of a rigid and resistant hair shaft through their extensive disulfide bond cross-linking with abundant cysteine residues of hair keratins. The matrix proteins include the high-sulfur and high-glycine-tyrosine keratins.[UniProtKB/Swiss-Prot Function]
  • Category: RNAi
  • Synonyms: KAP8.1
  • Sequences: Available with shipment
  • Stability: One year from date of shipment when stored at -20°C.
  • Components: KRTAP8-1 (Human) - 3 unique 27mer siRNA duplexes - 2 nmol each (Locus ID 337879)Included - SR30004, Trilencer-27 Universal Scrambled Negative Control siRNA Duplex - 2 nmolIncluded - SR30005, RNAse free siRNA Duplex Resuspension Buffer - 2 ml Need an individual siRNA?
  • Uniprot Id: Q8IUC2
  • Availability: 3 Weeks
  • Quality Control: Tested by ESI-MS
  • Performance Guaranteed: OriGene guarantees that at least two of the three Dicer-Substrate duplexes in the kit will provide at least 70% or more knockdown of the target mRNA when used at 10 nM concentration by quantitative RT-PCR when the TYE-563 fluorescent transfection control duplex (cat# SR30002) indicates that >90% of the cells have been transfected and the HPRT positive control (cat# SR30003) provides 90% knockdown efficiency. For non-conforming siRNA, requests for replacement product must be made within ninety (90) days from the date of delivery of the siRNA kit. To arrange for a free replacement with newly designed duplexes, please contact Technical Services at techsupport@origene.com. Please provide your data indicating the transfection efficiency and measurement of gene expression knockdown compared to the scrambled siRNA control (quantitative RT-PCR data required).
  • Number of Transfections: Approximately 330 transfections/2nmol in 24-well plate under optimized conditions (final conc. 10 nM).