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: 3 gene(s) found matching 'NBN'
Gene Symbol: NBN (Human)Other Aliases: AT-V1, AT-V2, ATV, NBS, NBS1, P95
Refseq IDs: NM_002485, XM_005250923, XR_242390, XR_242391
Description: Nibrin
Mutations in this gene are associated with Nijmegen breakage syndrome, an autosomal recessive chromosomal instability syndrome characterized by microcephaly, growth retardation, immunodeficiency, and cancer predisposition. The encoded protein is a member of the MRE11/RAD50 double-strand break repair complex which consists of 5 proteins. This gene product is thought to be involved in DNA double-strand break repair and DNA damage-induced checkpoint activation. Two alternatively spliced transcript variants encoding different isoforms have been found for this gene.
Products:
 RT˛ Profiler™ PCR Array6 products

Gene Symbol: SLC4A2 (Human)Other Aliases: AE2, BND3L, EPB3L1, HKB3, NBND3
Refseq IDs: NM_003040, NM_001199692, NM_001199693, NM_001199694, XM_005250041, XM_005250042, XR_242189
Description: Solute carrier family 4, anion exchanger, member 2 (erythrocyte membrane protein band 3-like 1)
Products:
 RT˛ Profiler™ PCR ArrayInquire

Gene Symbol: ARTN (Human)Other Aliases: ENOVIN, EVN, NBN
Refseq IDs: NM_057091, NM_057090, NM_001136215
Description: Artemin
The protein encoded by this gene is a member of the glial cell line-derived neurotophic factor (GDNF) family of ligands which are a group of ligands within the TGF-beta superfamily of signaling molecules. GDNFs are unique in having neurotrophic properties and have potential use for gene therapy in neurodegenrative disease. Artemin has been shown in culture to support the survival of a number of periferal neuron populations and at least one population of dopaminergic CNS neurons. Its role in the PNS and CNS is further substantiated by its expression pattern in the proximity of these neurons. This protein is a ligand for the RET receptor and uses GFR-alpha 3 as a coreceptor. Four alternatively spliced transcripts have been described, two of which encode the same protein.
Products:
 RT˛ Profiler™ PCR Array2 products