QIAGEN Website    Quick Order    Online Seminar    Contact    My Account
Home  >  Catalog  >  Browse Products By Gene

Browse Products By Gene


Search the entire catalog of SABiosciences products by gene name, key word, or RefSeq number. To learn more about all of these products, visit our Send an Email to Technical Support.

  1. Choose your species of interest first: Human, Mouse, Rat, Rhesus Macaque or Fruit Fly.
  2. Use Gene Symbols, key words, or RefSeq Accession Numbers for your gene of interest to find the catalog numbers for the corresponding products. To learn how to get RefSeq Accession Numbers, click here.
  3. Select the Product Line(s) that you would like to search.
  4. Click 'Submit'.
Species:
Gene Name, symbol, description:      RefSeq Number:   
All Product Lines
RT˛ Profiler™ PCR Array Pathway-Focused qRT-PCR Based Expression Profiling
RT˛ qPCR Primer Assay Gene-Specific Primers for qRT-PCR, Genome-Wide Availability
Cignal™ Pathway Reporter Assays Cell-Based Assays for Rapidly Analyzing Pathway Signaling Activity
miScript miRNA PCR Array miScript miRNA PCR Array
Multi-Analyte Profiler ELISArray Kits Analyze 12 Cytokines or Chemokines Simultaneously Using ELISA
Single Analyte ELISArray Kits High Performance ELISA with the Best Possible Antibodies
EpiTect Methyl II PCR Arrays Pathway-Focused PCR Based DNA Methylation Analysis
EpiTect Methyl II PCR Primer Assay PCR Assays for DNA Methylation Analysis, Genome-Wide Availability
SureSilencing™ shRNA Gene-Specific Plasmid-Based RNA Interference, Genome-Wide Availability
EpiTect ChIP qPCR Arrays Pathway-Focused qPCR Based Histone Modifications Analysis
        
Search Result: 2 gene(s) found matching 'WRN'
Gene Symbol: WRN (Human)Other Aliases: RECQ3, RECQL2, RECQL3
Refseq IDs: NM_000553, XM_005273632, ENST00000298139, ENST00000520169, ENST00000521620
Description: Werner syndrome, RecQ helicase-like
This gene encodes a member of the RecQ subfamily and the DEAH (Asp-Glu-Ala-His) subfamily of DNA and RNA helicases. DNA helicases are involved in many aspects of DNA metabolism, including transcription, replication, recombination, and repair. This protein contains a nuclear localization signal in the C-terminus and shows a predominant nucleolar localization. It possesses an intrinsic 3' to 5' DNA helicase activity, and is also a 3' to 5' exonuclease. Based on interactions between this protein and Ku70/80 heterodimer in DNA end processing, this protein may be involved in the repair of double strand DNA breaks. Defects in this gene are the cause of werner syndrome, an autosomal recessive disorder characterized by premature aging.
Products:
 RT˛ Profiler™ PCR Array2 products

Gene Symbol: WRNIP1 (Human)Other Aliases: RP11-420G6.2, WHIP, bA420G6.2
Refseq IDs: NM_020135, NM_130395, XM_005249232, XM_005249233, XM_005249234
Description: Werner helicase interacting protein 1
Werner's syndrome is a rare autosomal recessive disorder characterized by premature aging. The protein encoded by this gene interacts with the N-terminal portion of Werner protein containing the exonuclease domain. This protein shows homology to replication factor C family proteins, and is conserved from E. coli to human. Studies in yeast suggest that this gene may influence the aging process. Two transcript variants encoding different isoforms have been isolated for this gene.
Products:
 RT˛ Profiler™ PCR ArrayInquire