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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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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: 7 gene(s) found matching 'GP9'
Gene Symbol: GP9 (Human)Other Aliases: CD42a, GPIX
Refseq IDs: NM_000174, XM_005247374, XM_011512701, XM_011512702
Description: Glycoprotein IX (platelet)
Platelet glycoprotein IX (GP9) is a small membrane glycoprotein found on the surface of human platelets. It forms a 1-to-1 noncovalent complex with glycoprotein Ib (GP Ib), a platelet surface membrane glycoprotein complex that functions as a receptor for von Willebrand factor (VWF; MIM 193400). The main portion of the receptor is a heterodimer composed of 2 polypeptide chains, an alpha chain (GP1BA; MIM 606672) and a beta chain (GP1BB; MIM 138720), that are linked by disulfide bonds. The complete receptor complex includes noncovalent association of the alpha and beta subunits with GP9 and platelet glycoprotein V (GP5; MIM 173511).[supplied by OMIM]

Gene Symbol: HSP90B1 (Human)Other Aliases: ECGP, GP96, GRP94, HEL-S-125m, HEL35, TRA1
Refseq IDs: NM_003299, ENST00000299767, ENST00000540297, ENST00000548462, ENST00000548622, ENST00000549334, ENST00000550479, ENST00000550595, ENST00000551983, ENST00000552051
Description: Heat shock protein 90kDa beta (Grp94), member 1

Gene Symbol: NOX1 (Human)Other Aliases: GP91-2, MOX1, NOH-1, NOH1
Refseq IDs: NM_007052, NM_013955, NM_001271815
Description: NADPH oxidase 1
Voltage-gated proton (hydrogen) channels play an important role in cellular defense against acidic stress. They are unique among ion channels with respect to their extremely high selectivity, marked temperature dependence, and unitary conductance, which is 3 orders of magnitude lower than that of most other ion channels. NOX1 is a homolog of the catalytic subunit of the superoxide-generating NADPH oxidase of phagocytes, gp91phox. Three splice variants of NOX1 have been identified, NOH-1L, NOH-1S and NOH-1Lv. The NOH-1S currents were reversibly blocked by zinc, a known H+ channel inhibitor. The NOH-1S variant does not contain an electron transport chain and it is thought that H+ conductance is its main physiologic function, whereas NOH-1L may conduct H+ ions as part of its electron transport mechanism.

Gene Symbol: NOX3 (Human)Other Aliases: GP91-3, MOX-2
Refseq IDs: NM_015718
Description: NADPH oxidase 3
NADPH oxidases, such as NOX3, are plasma membrane-associated enzymes found in many cell types. They catalyze the production of superoxide by a 1-electron reduction of oxygen, using NADPH as the electron donor.[supplied by OMIM]

Gene Symbol: SORT1 (Human)Other Aliases: Gp95, LDLCQ6, NT3
Refseq IDs: NM_002959, NM_001205228, XM_005271100, XM_005271101, XM_005271102, ENST00000256637, ENST00000466471, ENST00000471996, ENST00000482236, ENST00000483508, ENST00000485149, ENST00000493736, ENST00000495777, ENST00000538502, XM_006710812
Description: Sortilin 1
This gene encodes a protein that is a multi-ligand type-1 receptor with similarity to the yeast carboxypeptidase Y sorting receptor Vps10 protein. The encoded protein, a trans-Golgi network (TGN) transmembrane protein, binds a number of unrelated ligands that participate in a wide range of cellular processes; however, it lacks the typical features of a signalling receptor. In the TGN, furin mediates the activation of the mature binding form. The encoded protein consists of a large luminal domain, a single transmembrane segment and short C-terminal cytoplasmic tail. The luminal domain contains a cysteine-rich region similar to two corresponding segments in the yeast Vps10p; the cytoplasmic tail is similar to the corresponding segment of the cation-independent mannose 6-phosphate receptor and the tail also interacts with the VHS domains of GGA (Golgi-associated, gamma-adaptin homologous, ARF-interacting) proteins.

Gene Symbol: LGALS3BP (Human)Other Aliases: 90K, BTBD17B, CyCAP, M2BP, MAC-2-BP, TANGO10B, gp90
Refseq IDs: NM_005567, ENST00000262776, ENST00000585407, ENST00000586300, ENST00000586720, ENST00000587251, ENST00000587310, ENST00000587311, ENST00000588198, ENST00000588205, ENST00000588508, ENST00000588587, ENST00000588899, ENST00000588990, ENST00000589527, ENST00000589775, ENST00000589906, ENST00000591274, ENST00000591778, ENST00000592255
Description: Lectin, galactoside-binding, soluble, 3 binding protein
The galectins are a family of beta-galactoside-binding proteins implicated in modulating cell-cell and cell-matrix interactions. LGALS3BP has been found elevated in the serum of patients with cancer and in those infected by the human immunodeficiency virus (HIV). It appears to be implicated in immune response associated with natural killer (NK) and lymphokine-activated killer (LAK) cell cytotoxicity. Using fluorescence in situ hybridization the full length 90K cDNA has been localized to chromosome 17q25. The native protein binds specifically to a human macrophage-associated lectin known as Mac-2 and also binds galectin 1.

Gene Symbol: CYBB (Human)Other Aliases: AMCBX2, CGD, GP91-1, GP91-PHOX, GP91PHOX, IMD34, NOX2, p91-PHOX
Refseq IDs: NM_000397, ENST00000378588, ENST00000492288, ENST00000536160, ENST00000545017, XM_011543890
Description: Cytochrome b-245, beta polypeptide
Cytochrome b (-245) is composed of cytochrome b alpha (CYBA) and beta (CYBB) chain. It has been proposed as a primary component of the microbicidal oxidase system of phagocytes. CYBB deficiency is one of five described biochemical defects associated with chronic granulomatous disease (CGD). In this disorder, there is decreased activity of phagocyte NADPH oxidase; neutrophils are able to phagocytize bacteria but cannot kill them in the phagocytic vacuoles. The cause of the killing defect is an inability to increase the cell's respiration and consequent failure to deliver activated oxygen into the phagocytic vacuole.