SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
TBX15-AP4B1-20-RERE | 20 (40 μL) | 200 μL | Request Pricing | |
TBX15-AP4B1-20-REOR | 20 (40 μL) | 200 μL | Request Pricing | |
TBX15-AP4B1-20-REGO | 20 (40 μL) | 200 μL | Request Pricing | |
TBX15-AP4B1-20-REGR | 20 (40 μL) | 200 μL | Request Pricing | |
TBX15-AP4B1-20-REAQ | 20 (40 μL) | 200 μL | Request Pricing | |
TBX15-AP4B1-20-ORRE | 20 (40 μL) | 200 μL | Request Pricing | |
TBX15-AP4B1-20-OROR | 20 (40 μL) | 200 μL | Request Pricing | |
TBX15-AP4B1-20-ORGO | 20 (40 μL) | 200 μL | Request Pricing | |
TBX15-AP4B1-20-ORGR | 20 (40 μL) | 200 μL | Request Pricing | |
TBX15-AP4B1-20-ORAQ | 20 (40 μL) | 200 μL | Request Pricing | |
TBX15-AP4B1-20-GORE | 20 (40 μL) | 200 μL | Request Pricing | |
TBX15-AP4B1-20-GOOR | 20 (40 μL) | 200 μL | Request Pricing | |
TBX15-AP4B1-20-GOGO | 20 (40 μL) | 200 μL | Request Pricing | |
TBX15-AP4B1-20-GOGR | 20 (40 μL) | 200 μL | Request Pricing | |
TBX15-AP4B1-20-GOAQ | 20 (40 μL) | 200 μL | Request Pricing | |
TBX15-AP4B1-20-GRRE | 20 (40 μL) | 200 μL | Request Pricing | |
TBX15-AP4B1-20-GROR | 20 (40 μL) | 200 μL | Request Pricing | |
TBX15-AP4B1-20-GRGO | 20 (40 μL) | 200 μL | Request Pricing | |
TBX15-AP4B1-20-GRGR | 20 (40 μL) | 200 μL | Request Pricing | |
TBX15-AP4B1-20-GRAQ | 20 (40 μL) | 200 μL | Request Pricing | |
TBX15-AP4B1-20-AQRE | 20 (40 μL) | 200 μL | Request Pricing | |
TBX15-AP4B1-20-AQOR | 20 (40 μL) | 200 μL | Request Pricing | |
TBX15-AP4B1-20-AQGO | 20 (40 μL) | 200 μL | Request Pricing | |
TBX15-AP4B1-20-AQGR | 20 (40 μL) | 200 μL | Request Pricing | |
TBX15-AP4B1-20-AQAQ | 20 (40 μL) | 200 μL | Request Pricing |
This gene belongs to the T-box family of genes, which encode a phylogenetically conserved family of transcription factors that regulate a variety of developmental processes. All these genes contain a common T-box DNA-binding domain. Mutations in this gene are associated with Cousin syndrome.[provided by RefSeq, Oct 2009]
Gene Symbol : TBX15
Gene Name : T-box 15
Chromosome : CHR 1: 118,989,555-118,883,042
Locus : 1p12
This gene encodes a subunit of a heterotetrameric adapter-like complex 4 that is involved in targeting proteins from the trans-Golgi network to the endosomal-lysosomal system. Mutations in this gene are associated with cerebral palsy spastic quadriplegic type 5 (CPSQ5) disorder. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]
Gene Symbol : AP4B1
Gene Name : Adaptor related protein complex 4 beta 1 subunit
Chromosome : CHR 1: 113,905,201-113,894,193
Locus : 1p13.2
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