The T-box (TBX) motif is present in a family of genes whose structural features and expression patterns support their involvement in developmental generegulation. The TBX gene family are largely conserved throughout metazoan evolution, and these genes code for putative transcription factors that share...
Gene ID (NCBI)9095 ConjugateUnconjugated FormLiquid Purification MethodAntigen affinity purification UNIPROT IDO60806 Storage BufferPBS with 0.02% sodium azide and 50% glycerol pH 7.3. Storage ConditionsStore at -20°C. Stable for one year after shipment.Aliquoting is unnecessary for -20oC storage.20...
The T-box (TBX) motif is present in a family of genes whose structural features and expression patterns support their involvement in developmental generegulation. The TBX gene family are largely conserved throughout metazoan evolution, and these genes code for putative transcription factors that share...
FormLiquid IsotypeIgG ConjugationUnconjugated StorageAliquot and store at -20°C. Avoid repeated freeze/thaw cycles. Molecular WeightCalculated MW: 48 kDa Observed MW: 48 kDa Swiss ProtO60806 GeneID9095 Gene SymbolTBX19 Concentration> 1 mg/ml ...
Long Gene nameT box 19 Synonymsdj747L4.1TPIT Synonyms nameTBS 19 GenBank acessionAJ010277 locos14.2 Discovery year1999-02-01 Pubmed identification9888994 RefSeq identitynnm_ Havana BLAST/blattothumg000034648 mesh Data ,Western 树号05.196.401.143E05.301.300.096E05.478.566.320.200E05.601.262E05.601....
Next, by luciferase reporter assays, we identified theTBX15regulatory region containing two functional NF-κB binding sites with response to NF-κBp65, mapping on the -3302 and -3059 positions of theTBX15gene. Moreover, a direct interaction of NF-κBp65 with one of the two NF-κB binding ...
The T-box (TBX) motif is present in a family of genes whose structural features and expression patterns support their involvement in developmental generegulation. The TBX gene family are largely conserved throughout metazoan evolution, and these genes code for putative transcription factors that share...
In conclusion, TBX19 gene analysis must be performed if adrenal insufficiency is associated with isolated ACTH deficiency. Delay in diagnosis may lead to inappropriate diagnoses, such as epilepsy, and thus inappropriate therapy, which may result in neonatal mortality. Unal, EdipDicle UnivYildirim, ...
TBX19geneHypoglycemiaIsolated ACTH deficiencyCongenital isolated adrenocorticotropic hormone (ACTH) deficiency (IAD) is a rarely seen disease characterized by low serum ACTH and cortisol levels accompanied by normal levels of the other anterior...
TBX19Isolated ACTH deficiencyGrowthPubertyCentral adrenal insufficiencyBackground Biallelic mutations in the TBX19gene cause severe early-onset adrenal failure due to isolated ACTH deficiency (IAD). This rare disease is characterized by low plasma ACTH and cortisol......