SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
TBL1XR1-DCUN1D1-20-RERE | 20 (40 μL) | 200 μL | Request Pricing | |
TBL1XR1-DCUN1D1-20-REOR | 20 (40 μL) | 200 μL | Request Pricing | |
TBL1XR1-DCUN1D1-20-REGO | 20 (40 μL) | 200 μL | Request Pricing | |
TBL1XR1-DCUN1D1-20-REGR | 20 (40 μL) | 200 μL | Request Pricing | |
TBL1XR1-DCUN1D1-20-REAQ | 20 (40 μL) | 200 μL | Request Pricing | |
TBL1XR1-DCUN1D1-20-ORRE | 20 (40 μL) | 200 μL | Request Pricing | |
TBL1XR1-DCUN1D1-20-OROR | 20 (40 μL) | 200 μL | Request Pricing | |
TBL1XR1-DCUN1D1-20-ORGO | 20 (40 μL) | 200 μL | Request Pricing | |
TBL1XR1-DCUN1D1-20-ORGR | 20 (40 μL) | 200 μL | Request Pricing | |
TBL1XR1-DCUN1D1-20-ORAQ | 20 (40 μL) | 200 μL | Request Pricing | |
TBL1XR1-DCUN1D1-20-GORE | 20 (40 μL) | 200 μL | Request Pricing | |
TBL1XR1-DCUN1D1-20-GOOR | 20 (40 μL) | 200 μL | Request Pricing | |
TBL1XR1-DCUN1D1-20-GOGO | 20 (40 μL) | 200 μL | Request Pricing | |
TBL1XR1-DCUN1D1-20-GOGR | 20 (40 μL) | 200 μL | Request Pricing | |
TBL1XR1-DCUN1D1-20-GOAQ | 20 (40 μL) | 200 μL | Request Pricing | |
TBL1XR1-DCUN1D1-20-GRRE | 20 (40 μL) | 200 μL | Request Pricing | |
TBL1XR1-DCUN1D1-20-GROR | 20 (40 μL) | 200 μL | Request Pricing | |
TBL1XR1-DCUN1D1-20-GRGO | 20 (40 μL) | 200 μL | Request Pricing | |
TBL1XR1-DCUN1D1-20-GRGR | 20 (40 μL) | 200 μL | Request Pricing | |
TBL1XR1-DCUN1D1-20-GRAQ | 20 (40 μL) | 200 μL | Request Pricing | |
TBL1XR1-DCUN1D1-20-AQRE | 20 (40 μL) | 200 μL | Request Pricing | |
TBL1XR1-DCUN1D1-20-AQOR | 20 (40 μL) | 200 μL | Request Pricing | |
TBL1XR1-DCUN1D1-20-AQGO | 20 (40 μL) | 200 μL | Request Pricing | |
TBL1XR1-DCUN1D1-20-AQGR | 20 (40 μL) | 200 μL | Request Pricing | |
TBL1XR1-DCUN1D1-20-AQAQ | 20 (40 μL) | 200 μL | Request Pricing |
Gene Symbol : DCUN1D1
Gene Name : Defective in cullin neddylation 1 domain containing 1
Chromosome : CHR 3: 182,986,363-182,938,157
Locus : 3q26.33
This gene is a member of the WD40 repeat-containing gene family and shares sequence similarity with transducin (beta)-like 1X-linked (TBL1X). The protein encoded by this gene is thought to be a component of both nuclear receptor corepressor (N-CoR) and histone deacetylase 3 (HDAC 3) complexes, and is required for transcriptional activation by a variety of transcription factors. Mutations in these gene have been associated with some autism spectrum disorders, and one finding suggests that haploinsufficiency of this gene may be a cause of intellectual disability with dysmorphism. Mutations in this gene as well as recurrent translocations involving this gene have also been observed in some tumors. [provided by RefSeq, Mar 2016]
Gene Symbol : TBL1XR1
Gene Name : Transducin beta like 1 X-linked receptor 1
Chromosome : CHR 3: 177,197,356-177,019,354
Locus : 3q26.32
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