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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.

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  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.
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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: 14 gene(s) found matching 'WAS'
Gene Symbol: WAS (Human)Other Aliases: IMD2, SCNX, THC, THC1, WASP
Refseq IDs: NM_000377
Description: Wiskott-Aldrich syndrome (eczema-thrombocytopenia)
The Wiskott-Aldrich syndrome (WAS) family of proteins share similar domain structure, and are involved in transduction of signals from receptors on the cell surface to the actin cytoskeleton. The presence of a number of different motifs suggests that they are regulated by a number of different stimuli, and interact with multiple proteins. Recent studies have demonstrated that these proteins, directly or indirectly, associate with the small GTPase, Cdc42, known to regulate formation of actin filaments, and the cytoskeletal organizing complex, Arp2/3. Wiskott-Aldrich syndrome is a rare, inherited, X-linked, recessive disease characterized by immune dysregulation and microthrombocytopenia, and is caused by mutations in the WAS gene. The WAS gene product is a cytoplasmic protein, expressed exclusively in hematopoietic cells, which show signalling and cytoskeletal abnormalities in WAS patients. A transcript variant arising as a result of alternative promoter usage, and containing a different 5' UTR sequence, has been described, however, its full-length nature is not known.
Products:
 RT˛ Profiler™ PCR Array3 products

Gene Symbol: WASF1 (Human)Other Aliases: SCAR1, WAVE, WAVE1
Refseq IDs: NM_003931, NM_001024934, NM_001024935, NM_001024936, XM_005267203, XM_005267204, XM_005267205, XM_005267206, XM_005267207, XM_005267208
Description: WAS protein family, member 1
The protein encoded by this gene, a member of the Wiskott-Aldrich syndrome protein (WASP)-family, plays a critical role downstream of Rac, a Rho-family small GTPase, in regulating the actin cytoskeleton required for membrane ruffling. It has been shown to associate with an actin nucleation core Arp2/3 complex while enhancing actin polymerization in vitro. Wiskott-Aldrich syndrome is a disease of the immune system, likely due to defects in regulation of actin cytoskeleton. Multiple alternatively spliced transcript variants encoding the same protein have been found for this gene.
Products:
 RT˛ Profiler™ PCR Array3 products

Gene Symbol: WASF2 (Human)Other Aliases: IMD2, SCAR2, WASF4, WAVE2, dJ393P12.2
Refseq IDs: NM_006990, NM_001201404
Description: WAS protein family, member 2
This gene encodes a member of the Wiskott-Aldrich syndrome protein family. The gene product is a protein that forms a multiprotein complex that links receptor kinases and actin. Binding to actin occurs through a C-terminal verprolin homology domain in all family members. The multiprotein complex serves to tranduce signals that involve changes in cell shape, motility or function. The published map location (PMID:10381382) has been changed based on recent genomic sequence comparisons, which indicate that the expressed gene is located on chromosome 1, and a pseudogene may be located on chromosome X.
Products:
 RT˛ Profiler™ PCR Array1 products

Gene Symbol: WASF3 (Human)Other Aliases: Brush-1, SCAR3, WAVE3
Refseq IDs: NM_006646, XM_005266239
Description: WAS protein family, member 3
This gene encodes a member of the Wiskott-Aldrich syndrome protein family. The gene product is a protein that forms a multiprotein complex that links receptor kinases and actin. Binding to actin occurs through a C-terminal verprolin homology domain in all family members. The multiprotein complex serves to tranduce signals that involve changes in cell shape, motility or function.
Products:
 RT˛ Profiler™ PCR Array1 products

Gene Symbol: WASF4P (Human)Other Aliases: WASF4
Refseq IDs: NM_001102604
Description: WAS protein family, member 4, pseudogene
Products:
 RT˛ Profiler™ PCR ArrayInquire

Gene Symbol: WASH1 (Human)Other Aliases: FAM39E, WASH
Refseq IDs: NM_182905, XM_005251335, XM_005251336, XR_242494
Description: WAS protein family homolog 1
Products:
 RT˛ Profiler™ PCR ArrayInquire

Gene Symbol: WASH2P (Human)Other Aliases: FAM39B
Refseq IDs: NR_024077
Description: WAS protein family homolog 2 pseudogene
Products:
 RT˛ Profiler™ PCR ArrayInquire

Gene Symbol: WASH3P (Human)Other Aliases: FAM39DP
Refseq IDs: NR_003659, XR_250570
Description: WAS protein family homolog 3 pseudogene
Products:
 RT˛ Profiler™ PCR ArrayInquire

Gene Symbol: WASH6P (Human)Other Aliases: CXYorf1, FAM39A, WASH
Refseq IDs: XM_377073
Description: WAS protein family homolog 6 pseudogene
Products:
 RT˛ Profiler™ PCR ArrayInquire

Gene Symbol: WASL (Human)Other Aliases: N-WASP, NWASP
Refseq IDs: NM_003941
Description: Wiskott-Aldrich syndrome-like
The Wiskott-Aldrich syndrome (WAS) family of proteins share similar domain structure, and are involved in transduction of signals from receptors on the cell surface to the actin cytoskeleton. The presence of a number of different motifs suggests that they are regulated by a number of different stimuli, and interact with multiple proteins. Recent studies have demonstrated that these proteins, directly or indirectly, associate with the small GTPase, Cdc42, known to regulate formation of actin filaments, and the cytoskeletal organizing complex, Arp2/3. The WASL gene product is a homolog of WAS protein, however, unlike the latter, it is ubiquitously expressed and shows highest expression in neural tissues. It has been shown to bind Cdc42 directly, and induce formation of long actin microspikes.
Products:
 RT˛ Profiler™ PCR Array4 products

Gene Symbol: WIPF1 (Human)Other Aliases: PRPL-2, WASPIP, WIP
Refseq IDs: NM_003387, NM_001077269, XM_005246834, XM_005246835
Description: WAS/WASL interacting protein family, member 1
This gene encodes a protein that plays an important role in the organization of the actin cytoskeleton. The encoded protein binds to a region of Wiskott-Aldrich syndrome protein that is frequently mutated in Wiskott-Aldrich syndrome, an X-linked recessive disorder. Impairment of the interaction between these two proteins may contribute to the disease. Alternative transcript variants exist for this gene, but their full-length natures have not been described.
Products:
 RT˛ Profiler™ PCR Array1 products

Gene Symbol: WIPF3 (Human)Other Aliases: CR16
Refseq IDs: NM_001080529, XM_005249822
Description: WAS/WASL interacting protein family, member 3
Products:
 RT˛ Profiler™ PCR ArrayInquire

Gene Symbol: WIPF2 (Human)Other Aliases: WICH, WIRE
Refseq IDs: NM_133264, XM_005257083, XM_005257084, XM_005257085, XM_005257086, XM_005257087
Description: WAS/WASL interacting protein family, member 2
This gene encodes a WASP interacting protein (WIP)-related protein. It has been shown that this protein has a role in the WASP-mediated organization of the actin cytoskeleton and that this protein is a potential link between the activated platelet-derived growth factor receptor and the actin polymerization machinery.
Products:
 RT˛ Profiler™ PCR ArrayInquire

Gene Symbol: NCKIPSD (Human)Other Aliases: AF3P21, DIP, DIP1, ORF1, SPIN90, VIP54, WASLBP, WISH
Refseq IDs: NM_184231, NM_016453, XM_005265222, XM_005265223
Description: NCK interacting protein with SH3 domain
The protein encoded by this gene is localized exclusively in the cell nucleus. It plays a role in signal transduction, and may function in the maintenance of sarcomeres and in the assembly of myofibrils into sarcomeres. It also plays an important role in stress fiber formation. The gene is involved in therapy-related leukemia by a chromosomal translocation t(3;11)(p21;q23) that involves this gene and the myeloid/lymphoid leukemia gene. Alternative splicing occurs in this locus and two transcript variants encoding distinct isoforms have been identified.
Products:
 RT˛ Profiler™ PCR ArrayInquire