| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| ARNTL-TEAD1-20-RERE | 20 (40 μL) | 200 μL |
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| ARNTL-TEAD1-20-REOR | 20 (40 μL) | 200 μL |
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| ARNTL-TEAD1-20-REGO | 20 (40 μL) | 200 μL |
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| ARNTL-TEAD1-20-REGR | 20 (40 μL) | 200 μL |
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| ARNTL-TEAD1-20-REAQ | 20 (40 μL) | 200 μL |
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| ARNTL-TEAD1-20-ORRE | 20 (40 μL) | 200 μL |
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| ARNTL-TEAD1-20-OROR | 20 (40 μL) | 200 μL |
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| ARNTL-TEAD1-20-ORGO | 20 (40 μL) | 200 μL |
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| ARNTL-TEAD1-20-ORGR | 20 (40 μL) | 200 μL |
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| ARNTL-TEAD1-20-ORAQ | 20 (40 μL) | 200 μL |
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| ARNTL-TEAD1-20-GORE | 20 (40 μL) | 200 μL |
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| ARNTL-TEAD1-20-GOOR | 20 (40 μL) | 200 μL |
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| ARNTL-TEAD1-20-GOGO | 20 (40 μL) | 200 μL |
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| ARNTL-TEAD1-20-GOGR | 20 (40 μL) | 200 μL |
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| ARNTL-TEAD1-20-GOAQ | 20 (40 μL) | 200 μL |
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| ARNTL-TEAD1-20-GRRE | 20 (40 μL) | 200 μL |
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| ARNTL-TEAD1-20-GROR | 20 (40 μL) | 200 μL |
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| ARNTL-TEAD1-20-GRGO | 20 (40 μL) | 200 μL |
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| ARNTL-TEAD1-20-GRGR | 20 (40 μL) | 200 μL |
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| ARNTL-TEAD1-20-GRAQ | 20 (40 μL) | 200 μL |
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| ARNTL-TEAD1-20-AQRE | 20 (40 μL) | 200 μL |
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| ARNTL-TEAD1-20-AQOR | 20 (40 μL) | 200 μL |
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| ARNTL-TEAD1-20-AQGO | 20 (40 μL) | 200 μL |
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| ARNTL-TEAD1-20-AQGR | 20 (40 μL) | 200 μL |
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| ARNTL-TEAD1-20-AQAQ | 20 (40 μL) | 200 μL |
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The protein encoded by this gene is a basic helix-loop-helix protein that forms a heterodimer with CLOCK. This heterodimer binds E-box enhancer elements upstream of Period (PER1, PER2, PER3) and Cryptochrome (CRY1, CRY2) genes and activates transcription of these genes. PER and CRY proteins heterodimerize and repress their own transcription by interacting in a feedback loop with CLOCK/ARNTL complexes. Defects in this gene have been linked to infertility, problems with gluconeogenesis and lipogenesis, and altered sleep patterns. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]
Gene Symbol : ARNTL
Gene Name : Aryl hydrocarbon receptor nuclear translocator like
Chromosome : CHR 11: 132,766,12-133,872,67
Locus : 11p15.3
This gene encodes a ubiquitous transcriptional enhancer factor that is a member of the TEA/ATTS domain family. This protein directs the transactivation of a wide variety of genes and, in placental cells, also acts as a transcriptional repressor. Mutations in this gene cause Sveinsson's chorioretinal atrophy. Additional transcript variants have been described but their full-length natures have not been experimentally verified. [provided by RefSeq, May 2010]
Gene Symbol : TEAD1
Gene Name : TEA domain transcription factor 1
Chromosome : CHR 11: 126,744,21-129,447,36
Locus : 11p15.3
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