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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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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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	All Product Lines

	RT² Profiler™ PCR Array	Pathway-Focused qRT-PCR Based Expression Profiling
	RT² 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: 26 gene(s) found matching 'FUS'

Gene Symbol: FUS (Human)	Other Aliases: ALS6, FUS1, HNRNPP2, POMP75, TLS
Refseq IDs: NM_004960, NM_001170634, NM_001170937, NR_028388
Description: Fused in sarcoma

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RT² Profiler™ PCR Array

2 products

Gene Symbol: ATF1 (Human)	Other Aliases: ATF-1, EWS-ATF1, FUS, TREB36
Refseq IDs: NM_005171
Description: Activating transcription factor 1

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RT² Profiler™ PCR Array

4 products

Gene Symbol: NAT6 (Human)	Other Aliases: FUS-2, FUS2
Refseq IDs: NM_012191, NM_001200016, NM_001200018
Description: N-acetyltransferase 6 (GCN5-related)

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Gene Symbol: SKOR1 (Human)	Other Aliases: CORL1, FUSSEL15, LBXCOR1
Refseq IDs: NM_001031807
Description: SKI family transcriptional corepressor 1

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Gene Symbol: SKOR2 (Human)	Other Aliases: CORL2, FUSSEL18
Refseq IDs: XM_001715219
Description: SKI family transcriptional corepressor 2

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RT² Profiler™ PCR Array

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Gene Symbol: SRSF10 (Human)	Other Aliases: DKFZp686H0644, FLJ30749, FLJ43846, FUSIP1, FUSIP2, NSSR, SFRS13, SFRS13A, SRp38, SRrp40, TASR, TASR1, TASR2
Refseq IDs: NM_054016, NM_006625, NM_001191005, NM_001191006, NM_001191007, NM_001191009, NR_034035
Description: Serine/arginine-rich splicing factor 10
This gene product is a member of the serine-arginine (SR) family of proteins, which is involved in constitutive and regulated RNA splicing. Members of this family are characterized by N-terminal RNP1 and RNP2 motifs, which are required for binding to RNA, and multiple C-terminal SR/RS repeats, which are important in mediating association with other cellular proteins. This protein can influence splice site selection of adenovirus E1A pre-mRNA. It interacts with the oncoprotein TLS, and abrogates the influence of TLS on E1A pre-mRNA splicing. Alternative splicing of this gene results in at least two transcript variants encoding different isoforms. In addition, transcript variants utilizing alternative polyA sites exist.
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RT² Profiler™ PCR Array

1 products

Gene Symbol: TUSC2 (Human)	Other Aliases: C3orf11, FUS1, PAP, PDAP2
Refseq IDs: NM_007275
Description: Tumor suppressor candidate 2
This gene is a highly conserved lung cancer candidate gene. No other information about this gene is currently available.
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RT² Profiler™ PCR Array

2 products

Gene Symbol: UFD1L (Human)	Other Aliases: UFD1
Refseq IDs: NM_005659, NM_001035247
Description: Ubiquitin fusion degradation 1 like (yeast)
The protein encoded by this gene forms a complex with two other proteins, NPL4 and VCP, that is necessary for the degradation of ubiquitinated proteins. In addition, this complex controls the disassembly of the mitotic spindle and the formation of a closed nuclear envelope after mitosis. Mutations in this gene have been associated with Catch 22 syndrome as well as cardiac and craniofacial defects. Alternative splicing results in multiple transcript variants encoding different isoforms.
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RT² Profiler™ PCR Array

2 products

Gene Symbol: UBA52 (Human)	Other Aliases: CEP52, HUBCEP52, L40, MGC126879, MGC126881, MGC57125, RPL40
Refseq IDs: NM_003333, NM_001033930
Description: Ubiquitin A-52 residue ribosomal protein fusion product 1
Ubiquitin is a highly conserved nuclear and cytoplasmic protein that has a major role in targeting cellular proteins for degradation by the 26S proteosome. It is also involved in the maintenance of chromatin structure, the regulation of gene expression, and the stress response. Ubiquitin is synthesized as a precursor protein consisting of either polyubiquitin chains or a single ubiquitin moiety fused to an unrelated protein. This gene encodes a fusion protein consisting of ubiquitin at the N terminus and ribosomal protein L40 at the C terminus, a C-terminal extension protein (CEP). Multiple processed pseudogenes derived from this gene are present in the genome.
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Gene Symbol: TFPT (Human)	Other Aliases: FB1, INO80F, amida
Refseq IDs: NM_013342
Description: TCF3 (E2A) fusion partner (in childhood Leukemia)

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Gene Symbol: TFG (Human)	Other Aliases: FLJ36137, TF6, TRKT3
Refseq IDs: NM_006070, NM_001007565, NM_001195478, NM_001195479
Description: TRK-fused gene

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RT² Profiler™ PCR Array

1 products

Gene Symbol: SUFU (Human)	Other Aliases: PRO1280, SUFUH, SUFUXL
Refseq IDs: NM_016169, NM_001178133
Description: Suppressor of fused homolog (Drosophila)
SUFU encodes a component of the sonic hedgehog (SHH; MIM 600725)/patched (PTCH; MIM 601309) signaling pathway. Mutations in genes encoding components of this pathway are deleterious for normal development and are associated with cancer-predisposing syndromes (e.g., HPE3, MIM 142945; BCNS, MIM 109400; and GCPS, MIM 175700).[supplied by OMIM]
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RT² Profiler™ PCR Array

4 products

Gene Symbol: SETMAR (Human)	Other Aliases: METNASE
Refseq IDs: NM_006515, NR_024022
Description: SET domain and mariner transposase fusion gene

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Gene Symbol: RLF (Human)	Other Aliases: MGC142226, ZN-15L, ZNF292L
Refseq IDs: NM_012421
Description: Rearranged L-myc fusion

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RT² Profiler™ PCR Array

2 products

Gene Symbol: POMZP3 (Human)	Other Aliases: MGC8359, POM-ZP3, POM121
Refseq IDs: NM_012230, NM_152992
Description: POM121 and ZP3 fusion
This gene appears to have resulted from a fusion of DNA sequences derived from 2 distinct loci, specifically through the duplication of two internal exons from the POM121 gene and four 3' exons from the ZP3 gene. The 5' end of this gene is similar to the 5` coding region of the POM121 gene which encodes an integral nuclear pore membrane protein. However, the protein encoded by this gene lacks the nuclear pore localization motif. The 3' end of this gene is similar to the last 4 exons of the zona pellucida glycoprotein 3 (ZP3) gene and the encoded protein retains one zona pellucida domain. Multiple protein isoforms are encoded by transcript variants of this gene.
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RT² Profiler™ PCR Array

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Gene Symbol: LNP1 (Human)	Other Aliases:
Refseq IDs: NM_001085451
Description: Leukemia NUP98 fusion partner 1

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RT² Profiler™ PCR Array

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Gene Symbol: LHFPL5 (Human)	Other Aliases: DFNB67, MGC33835, TMHS, dJ510O8.8
Refseq IDs: NM_182548
Description: Lipoma HMGIC fusion partner-like 5
This gene is a member of the lipoma HMGIC fusion partner (LHFP) gene family, which is a subset of the superfamily of tetraspan transmembrane protein encoding genes. Mutations in this gene result in deafness in humans, and a mutation in a similar gene in mice results in deafness and vestibular dysfunction with severe degeneration of the organ of Corti. It is proposed to function in hair bundle morphogenesis.
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RT² Profiler™ PCR Array

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Gene Symbol: LHFPL4 (Human)	Other Aliases: MGC133162
Refseq IDs: NM_198560
Description: Lipoma HMGIC fusion partner-like 4
This gene is a member of the lipoma HMGIC fusion partner (LHFP) gene family, which is a subset of the superfamily of tetraspan transmembrane protein encoding genes. Mutations in one LHFP-like gene result in deafness in humans and mice, and a second LHFP-like gene is fused to a high-mobility group gene in a translocation-associated lipoma.
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RT² Profiler™ PCR Array

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Gene Symbol: LHFPL3 (Human)	Other Aliases: LHFPL4
Refseq IDs: NM_199000
Description: Lipoma HMGIC fusion partner-like 3
This gene is a member of the lipoma HMGIC fusion partner (LHFP) gene family, which is a subset of the superfamily of tetraspan transmembrane protein encoding genes. Mutations in one LHFP-like gene result in deafness in humans and mice, and a second LHFP-like gene is fused to a high-mobility group gene in a translocation-associated lipoma. A partial gene fragment named LHFPL4 corresponds to a portion of the first exon of this gene.
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Gene Symbol: LHFPL2 (Human)	Other Aliases: DKFZp781E0375, KIAA0206
Refseq IDs: NM_005779
Description: Lipoma HMGIC fusion partner-like 2
This gene is a member of the lipoma HMGIC fusion partner (LHFP) gene family, which is a subset of the superfamily of tetraspan transmembrane protein encoding genes. Mutations in one LHFP-like gene result in deafness in humans and mice, and a second LHFP-like gene is fused to a high-mobility group gene in a translocation-associated lipoma. Alternatively spliced transcript variants have been found, but their biological validity has not been determined.
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RT² Profiler™ PCR Array

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Gene Symbol: LHFPL1 (Human)	Other Aliases: MGC118798, MGC118800, MGC118801
Refseq IDs: NM_178175
Description: Lipoma HMGIC fusion partner-like 1
This gene is a member of the lipoma HMGIC fusion partner (LHFP) gene family, which is a subset of the superfamily of tetraspan transmembrane protein encoding genes. Mutations in one LHFP-like gene result in deafness in humans and mice, and a second LHFP-like gene is fused to a high-mobility group gene in a translocation-associated lipoma. Alternatively spliced transcript variants have been found, but their biological validity has not been determined.
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Gene Symbol: LHFP (Human)	Other Aliases: MGC22429
Refseq IDs: NM_005780
Description: Lipoma HMGIC fusion partner
This gene is a member of the lipoma HMGIC fusion partner (LHFP) gene family, which is a subset of the superfamily of tetraspan transmembrane protein encoding genes. This gene is fused to a high-mobility group gene in a translocation-associated lipoma. Mutations in another LHFP-like gene result in deafness in humans and mice. Alternatively spliced transcript variants have been found; however, their full-length nature is not known.
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Gene Symbol: IZUMO1 (Human)	Other Aliases: FLJ61440, IZUMO, MGC34799
Refseq IDs: NM_182575
Description: Izumo sperm-egg fusion 1
The sperm-specific protein Izumo, named for a Japanese shrine dedicated to marriage, is essential for sperm-egg plasma membrane binding and fusion (Inoue et al., 2005).[supplied by OMIM]
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Gene Symbol: FUBP3 (Human)	Other Aliases: FBP3, FLJ25229
Refseq IDs: NM_003934
Description: Far upstream element (FUSE) binding protein 3

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Gene Symbol: FUBP1 (Human)	Other Aliases: FBP, FUBP
Refseq IDs: NM_003902
Description: Far upstream element (FUSE) binding protein 1
This gene encodes a ssDNA binding protein that activates the far upstream element (FUSE) of c-myc and stimulates expression of c-myc in undifferentiated cells. Regulation of FUSE by FUBP occurs through single-strand binding of FUBP to the non-coding strand. This protein has been shown to function as an ATP-dependent DNA helicase.
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Gene Symbol: CHRFAM7A (Human)	Other Aliases: CHRNA7, CHRNA7-DR1, D-10, MGC120482, MGC120483
Refseq IDs: NM_148911, NM_139320
Description: CHRNA7 (cholinergic receptor, nicotinic, alpha 7, exons 5-10) and FAM7A (family with sequence similarity 7A, exons A-E) fusion
The nicotinic acetylcholine receptors (nAChRs) are members of a superfamily of ligand-gated ion channels that mediate fast signal transmission at synapses. The family member CHRNA7, which is located on chromosome 15 in a region associated with several neuropsychiatric disorders, is partially duplicated and forms a hybrid with a novel gene from the family with sequence similarity 7 (FAM7A). Alternative splicing has been observed, and two variants exist, for this hybrid gene. The N-terminally truncated products predicted by the largest open reading frames for each variant would lack the majority of the neurotransmitter-gated ion-channel ligand binding domain but retain the transmembrane region that forms the ion channel. Although current evidence supports transcription of this hybrid gene, translation of the nicotinic acetylcholine receptor-like protein-encoding open reading frames has not been confirmed.
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