TBX3 Antibody, HRP conjugated

說明書

中文名稱：

TBX3兔多克隆抗體, HRP偶聯
貨號：

CSB-PA023255LB01HU
規格：

￥880
其他：

產品詳情
產品評價
相關產品
靶點詳情

產品詳情

產品名稱：

Rabbit anti-Homo sapiens (Human) TBX3 Polyclonal antibody
Uniprot No.：

O15119
基因名：

TBX3
別名：

Bladder cancer related protein XHL antibody; T box 3 antibody; T-box protein 3 antibody; T-box transcription factor TBX3 antibody; Tbx3 antibody; TBX3 ISO antibody; TBX3_HUMAN antibody; UMS antibody; XHL antibody
宿主：

Rabbit
反應種屬：

Human
免疫原：

Recombinant Human T-box transcription factor TBX3 protein (297-479AA)
免疫原種屬：

Homo sapiens (Human)
標記方式：

HRP
克隆類型：

Polyclonal
抗體亞型：

IgG
純化方式：

>95%, Protein G purified
濃度：

It differs from different batches. Please contact us to confirm it.
保存緩沖液：

Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
產品提供形式：

Liquid
應用范圍：

ELISA
Protocols：

ELISA Protocol
儲存條件：

Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
貨期：

Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
用途：

For Research Use Only. Not for use in diagnostic or therapeutic procedures.

產品評價

靶點詳情

功能：

Transcriptional repressor involved in developmental processes. Binds to the palindromic T site 5'-TTCACACCTAGGTGTGAA-3' DNA sequence, or a half-site, which are present in the regulatory region of several genes. Probably plays a role in limb pattern formation. Required for mammary placode induction, and maintenance of the mammary buds during development. Involved in branching morphogenesis in both developing lungs and adult mammary glands, via negative modulation of target genes; acting redundantly with TBX2. Required, together with TBX2, to maintain cell proliferation in the embryonic lung mesenchyme; perhaps acting downstream of SHH, BMP and TGFbeta signaling. Involved in modulating early inner ear development, acting independently of, and also redundantly with, TBX2 in different subregions of the developing ear. Acts as a negative regulator of PML function in cellular senescence.
基因功能參考文獻：
1. TBX3 is not only required for development of posterior forelimb bones (ulna and digits 4 and 5), but also for a subset of posterior muscles (lateral triceps and brachialis) and their bone eminence attachment sites. PMID: 27491074
2. High TBX3 expression is associated with invasive breast cancer. PMID: 27553211
3. genetic variation of Tbx3 is associated with left ventricular mass in a healthy Japanese population [meta-analysis] PMID: 27195777
4. Study demonstrates that miR-206 directly targets Tbx3, that miR-206 and Tbx3 mRNA are inversely correlated in human breast cancer and that Tbx3 repression is necessary to elicit a significant functional effect of miR-206 in breast cancer cells. PMID: 27100732
5. The c.1423C>T (p.Q475*) nonsense mutation in exon 6 of the TBX3 gene associated with ulnar-mammary syndrome. PMID: 28145909
6. Tbx3 was found to be overexpressed in 46 of 98 human gastric cancer samples PMID: 27553355
7. Paracrine WNT signaling is stimulated by estrogen and progesterone, while autocrine WNT signaling is induced by the embryonic T-box transcription factor TBX3 PMID: 25350852
8. Overexpression of Tbx3 is associated with pancreatic carcinoma. PMID: 25743805
9. Polymorphisms in several genes involved in the Wnt signaling pathway were associated with hepatic fibrosis or inflammation risk in HCV-infected males. PMID: 24386373
10. TBX3 gene variants may contribute to indirect inguinal hernia as a rare risk factor by reducing TBX3 levels PMID: 25455105
11. An enhancement in TBX3 protein expression both in glomerular and tubular regions. PMID: 25158279
12. The pleiotropic effects of TBX3 mutations in humans and mice likely result from disrupting at least two molecular functions of this protein: transcriptional regulation and pre-mRNA splicing. PMID: 24675841
13. TBX3 may play an important role as a reciprocal switch between substrate dependent cell proliferation and tumour invasion. PMID: 24098938
14. TBX3 plays a pivotal role in mediating the antiproliferative and promigratory role of TGF-beta1 in breast epithelial cells and skin keratinocytes. PMID: 24025717
15. TBX3 exon 2 mutation is rare in most human tumors PMID: 23656610
16. Oncogenic B-RAF(V600E) signaling induces the T-Box3 transcriptional repressor to repress E-cadherin and enhance melanoma cell invasion. PMID: 23190890
17. TBX3 gene polymorphism is associated in the development of colorectal cancers. PMID: 23266556
18. Data show that Tbx3 is up-regulated in tissue samples of head and neck squamous cell cancer (HNSCC) patients and that Tbx3 represses PTEN transcription. PMID: 23082988
19. the sequence variants within the TBX3 gene promoter did not contribute to VSD etiology. PMID: 23116943
20. TBX3 promotes human embryonic stem cell proliferation and neuroepithelial differentiation in a differentiation stage-dependent manner. PMID: 22865636
21. TBX3 CPG island methylation predicts progression in bladder cancer. PMID: 22284968
22. Tbx3 overexpression promotes squamous carcinoma cell survival displaying an epithelial-mesenchymal transition phenotype. PMID: 22154512
23. In situ hybridization reveals Tbx3 and Sox4 to co-localize extensively in the embryo including the atrioventricular and outflow tract cushion mesenchyme and a small area of interventricular myocardium. PMID: 21538160
24. identify a Sp1 element and two CCAAT boxes to be essential for basal TBX3 promoter activity PMID: 21784138
25. Study indicate mutation of TBX3 gene in the family. PMID: 21199695
26. Tbx3 expression was found to be suppressed by AFLL when the expression of tumor suppressor genes p14 and p53 were activated PMID: 20702496
27. Data show that estrogen signaling expands the pool of functional breast cancer stem-like cells through a paracrine FGF/FGFR/Tbx3 signaling pathway. PMID: 21098263
28. pathway that up-regulates TBX3 expression and provides additional evidence that increased levels of TBX3 contribute to metastasis. PMID: 20942798
29. TBX3 mRNA expression was significantly higher in metastatic breast cancer than in non-metastatic tumors. PMID: 19218121
30. Studies identified Tbx3 as a key regulator of the SAN phenotype. PMID: 20133910
31. The mRNA and protein expressions of Tbx3 are markedly upregulated in breast cancer cell lines and tissue samples. PMID: 19403417
32. Mutations in Tbx3 are responsible for ulnar-mammary syndrome (UMS), an autosomal dominant disorder affecting limb, tooth, hair, apocrine gland and genital development. PMID: 11689487
33. Results demonstrate the structural consequences of T-box domain protein 3 point mutations observed in Ulnar-Mammary syndrome and Holt-Oram syndrome patients. PMID: 12005433
34. The results are consistent with the previous finding that UMS is caused by haploinsufficiency of TBX3. PMID: 12116211
35. Overexpression of TBX3 is associated with breast cancer PMID: 15289316
36. increased expression of truncated cSHMT, Tbx3 and utrophin in plasma samples obtained from patients at early stages of ovarian cancer and breast cancer PMID: 16049973
37. A literature review of TBX3 combined with a novel TBX3 mutation in a family with ulnar-mammary syndrome finds an association in mutations that disrupt the TBX3 DNA-binding domain and a higher frequency of severe upper limb malformations and teeth defects. PMID: 16530712
38. Required for heart and limb formation, and is mutated in ulnar-mammary syndrome. PMID: 16556916
39. Data show that Tbx3 plays an important role in osteogenic differentiation and proliferation of human mesenchymal stem cells derived from adipose tissue. PMID: 16955224
40. Nyx2-5 confines recombinant hTBX3 expression to the sinoatrial node & sinus horns in mice. Tbx3 suppresses chamber differentiation--another mechanism by which the Tbx3-positive sinoatrial node is shielded from differentiating into atrial myocardium. PMID: 17234970
41. TBX3 repression to its targets is dependent on HDAC activity. TBX3 may serve as a biomarker for breast cancer. PMID: 18245468
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相關疾病：

Ulnar-mammary syndrome (UMS)
亞細胞定位：

Nucleus.
組織特異性：

Widely expressed.
數據庫鏈接：

HGNC: 11602

OMIM: 181450

KEGG: hsa:6926

STRING: 9606.ENSP00000257566

UniGene: Hs.744016

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