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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: 4 gene(s) found matching 'CAV3'
Gene Symbol: CAV3 (Human)Other Aliases: LGMD1C, LQT9, VIP-21, VIP21
Refseq IDs: NM_001234, NM_033337, ENST00000343849, ENST00000397368, ENST00000472766
Description: Caveolin 3
This gene encodes a caveolin family member, which functions as a component of the caveolae plasma membranes found in most cell types. Caveolin proteins are proposed to be scaffolding proteins for organizing and concentrating certain caveolin-interacting molecules. Mutations identified in this gene lead to interference with protein oligomerization or intra-cellular routing, disrupting caveolae formation and resulting in Limb-Girdle muscular dystrophy type-1C (LGMD-1C), hyperCKemia or rippling muscle disease (RMD). Alternative splicing has been identified for this locus, with inclusion or exclusion of a differentially spliced intron. In addition, transcripts utilize multiple polyA sites and contain two potential translation initiation sites.
 RT˛ Profiler™ PCR Array4 products

Gene Symbol: CACNA1I (Human)Other Aliases: Cav3.3, ca(v)3.3
Refseq IDs: NM_021096, NM_001003406, ENST00000336649, ENST00000400164, ENST00000401624, ENST00000402142, ENST00000404898, ENST00000407673, ENST00000471970
Description: Calcium channel, voltage-dependent, T type, alpha 1I subunit
Voltage-dependent calcium channels control the rapid entry of Ca(2+) into a variety of cell types and are therefore involved in both electrical and cellular signaling. T-type channels, such as CACNA1I, are activated by small membrane depolarizations and can generate burst firing and pacemaker activity.[supplied by OMIM]
 RT˛ Profiler™ PCR Array1 products

Gene Symbol: CACNA1H (Human)Other Aliases: CACNA1HB, Cav3.2, ECA6, EIG6
Refseq IDs: NM_021098, NM_001005407, XM_005255652, XM_005255653, XM_005255654, XM_005255655, XM_005255656, XM_005255657, ENST00000348261, ENST00000358590, ENST00000562079, ENST00000564231, ENST00000564927, ENST00000564954, ENST00000565831, ENST00000569107, ENST00000569953
Description: Calcium channel, voltage-dependent, T type, alpha 1H subunit
This gene encodes a T-type member of the alpha-1 subunit family, a protein in the voltage-dependent calcium channel complex. Calcium channels mediate the influx of calcium ions into the cell upon membrane polarization and consist of a complex of alpha-1, alpha-2/delta, beta, and gamma subunits in a 1:1:1:1 ratio. The alpha-1 subunit has 24 transmembrane segments and forms the pore through which ions pass into the cell. There are multiple isoforms of each of the proteins in the complex, either encoded by different genes or the result of alternative splicing of transcripts. Alternate transcriptional splice variants, encoding different isoforms, have been characterized for the gene described here. Studies suggest certain mutations in this gene lead to childhood absence epilepsy (CAE).
 RT˛ Profiler™ PCR ArrayInquire

Gene Symbol: CACNA1G (Human)Other Aliases: Ca(V)T.1, Cav3.1, NBR13
Refseq IDs: NM_198397, NM_198396, NM_198388, NM_198387, NM_198386, NM_198385, NM_198384, NM_198383, NM_198382, NM_198380, NM_198379, NM_198378, NM_198377, NM_198376, NM_018896, NM_001256324, NM_001256325, NM_001256326, NM_001256327, NM_001256328, NM_001256329, NM_001256330, NM_001256331, NM_001256332, NM_001256333, NM_001256334, NM_001256359, NM_001256360, NM_001256361, NR_046054, NR_046055, NR_046056, NR_046057, NR_046058, ENST00000352832, ENST00000354983, ENST00000358244, ENST00000359106, ENST00000360761, ENST00000416767, ENST00000429973, ENST00000442258, ENST00000502264, ENST00000503436, ENST00000503485, ENST00000503607, ENST00000504076, ENST00000505165, ENST00000506406, ENST00000506520, ENST00000507336, ENST00000507510, ENST00000507609, ENST00000507896, ENST00000510115, ENST00000510366, ENST00000511765, ENST00000511768, ENST00000512389, ENST00000513689, ENST00000513964, ENST00000514079, ENST00000514181, ENST00000514717, ENST00000515165, ENST00000515411, ENST00000515765, ENST00000570567
Description: Calcium channel, voltage-dependent, T type, alpha 1G subunit
Voltage-activated calcium channels can be distinguished based on their voltage-dependence, deactivation, and single-channel conductance. See MIM 601011. Low-voltage-activated calcium channels are referred to as 'T' type because their currents are both transient, owing to fast inactivation, and tiny, owing to small conductance. T-type channels are thought to be involved in pacemaker activity, low-threshold calcium spikes, neuronal oscillations and resonance, and rebound burst firing.[supplied by OMIM]
 RT˛ Profiler™ PCR Array1 products