Anti-T Antibody (CAB16887)
- SKU:
- CAB16887
- Product type:
- Antibody
- Reactivity:
- Human
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
- Research Area:
- Epigenetics and Nuclear Signaling
Frequently bought together:
Description
| 抗体名: | Anti-T Antibody |
| 抗体コード: | CAB16887 |
| 抗体サイズ: | 20uL, 50uL, 100uL |
| 申し込み: | WB |
| 反応性: | Human |
| 宿主種: | Rabbit |
| 免疫原: | Recombinant fusion protein containing a sequence corresponding to amino acids 226-435 of human T (NP_003172.1). |
| 申し込み: | WB |
| 推奨希釈: | WB 1:500 - 1:1000 |
| 反応性: | Human |
| ポジティブサンプル: | H460 |
| 免疫原: | Recombinant fusion protein containing a sequence corresponding to amino acids 226-435 of human T (NP_003172.1). |
| 精製方法: | Affinity purification |
| ストレージバッファ: | Store at -20'C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
| アイソタイプ: | IgG |
| 順序: | HKEM MEEP GDSQ QPGY SQWG WLLP GTST LCPP ANPH PQFG GALS LPST HSCD RYPT LRSH RSSP YPSP YAHR NNSP TYSD NSPA CLSM LQSH DNWS SLGM PAHP SMLP VSHN ASPP TSSS QYPS LWSV SNGA VTPG SQAA AVSN GLGA QFFR GSPA HYTP LTHP VSAP SSSG SPLY EGAA AATD IVDS QYDA AAQG RLIA SWTP VSPP SM |
| 遺伝子ID: | 6862 |
| Uniprot: | O15178 |
| セルラーロケーション: | Nucleus |
| 計算された分子量: | 41kDa/47kDa |
| 観察された分子量: | 47kDa |
| 同義語: | T, SAVA, TFT |
| バックグラウンド: | The protein encoded by this gene is an embryonic nuclear transcription factor that binds to a specific DNA element, the palindromic T-site. It binds through a region in its N-terminus, called the T-box, and effects transcription of genes required for mesoderm formation and differentiation. The protein is localized to notochord-derived cells. Two transcript variants encoding different isoforms have been found for this gene. |
| UniProt Protein Function: | Brachyury: Involved in the transcriptional regulation of genes required for mesoderm formation and differentiation. Binds to a palindromic site (called T site) and activates gene transcription when bound to such a site. Genetic variations in T are associated with susceptibility to neural tube defects (NTD). NTD are common congenital malformations. Spina bifida, which results from malformations in the caudal region of the neural tube, is compatible with life but associated with significant morbidity, including lower limb paralysis. T is involved in susceptibility to the development of chordoma (CHDM). Chordomas are rare, clinically malignant tumors derived from notochordal remnants. They occur along the length of the spinal axis, predominantly in the sphenooccipital, vertebral and sacrococcygeal regions. They are characterized by slow growth, local destruction of bone, extension into adjacent soft tissues and rarely, distant metastatic spread. Susceptibility to development of chordomas is due to a T gene duplication. |
| UniProt Protein Details: | Protein type:Motility/polarity/chemotaxis; DNA-binding; Cell cycle regulation; Transcription factor Chromosomal Location of Human Ortholog: 6q27 Cellular Component: cytoplasm; nuclear chromatin; nucleus Molecular Function:RNA polymerase II transcription factor activity, enhancer binding; transcription factor activity Biological Process: transcription from RNA polymerase II promoter; heart morphogenesis; somitogenesis; neural plate morphogenesis; embryonic skeletal development; mesoderm migration; notochord formation; negative regulation of transcription from RNA polymerase II promoter; Wnt receptor signaling pathway through beta-catenin; signal transduction; BMP signaling pathway; determination of anterior/posterior axis, embryo; positive regulation of cell proliferation; neural tube closure; penetration of zona pellucida; mesoderm development; vasculogenesis Disease: Neural Tube Defects; Sacral Agenesis With Vertebral Anomalies |
| NCBI Summary: | The protein encoded by this gene is an embryonic nuclear transcription factor that binds to a specific DNA element, the palindromic T-site. It binds through a region in its N-terminus, called the T-box, and effects transcription of genes required for mesoderm formation and differentiation. The protein is localized to notochord-derived cells. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2012] |
| UniProt Code: | O15178 |
| NCBI GenInfo Identifier: | 4507339 |
| NCBI Gene ID: | 6862 |
| NCBI Accession: | NP_003172.1 |
| UniProt Secondary Accession: | O15178,Q4KMP4, E7ERD6, |
| UniProt Related Accession: | O15178 |
| Molecular Weight: | 41,078 Da |
| NCBI Full Name: | brachyury protein isoform 1 |
| NCBI Synonym Full Names: | T brachyury transcription factor |
| NCBI Official Symbol: | T |
| NCBI Official Synonym Symbols: | TFT; SAVA |
| NCBI Protein Information: | brachyury protein |
| UniProt Protein Name: | Brachyury protein |
| UniProt Synonym Protein Names: | Protein T |
| Protein Family: | THP3 |
| UniProt Gene Name: | T |
| UniProt Entry Name: | BRAC_HUMAN |
 | Western blot analysis of extracts of H460 cells, using T antibody (CAB16887) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) (CABS014) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit (RM00020). Exposure time: 30s. |
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