anti-T-Box 19 (TBX19) 抗体

TBX19 is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. 再加上,我们可以发T-Box 19 蛋白 (3)和数多这个蛋白质的别的产品。

列出全部抗体 基因 基因ID UniProt
TBX19 9095 O60806
TBX19 83993 Q99ME7
TBX19 304935  
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Showing 10 out of 15 products:

产品编号 适用 宿主 标记 应用范围 图像 规格 供应商 交付 价格 详细
Cow 非结合性 WB WB Suggested Anti-TBX19 Antibody Titration:  0.2-1 ug/ml  ELISA Titer:  1:1562500  Positive Control:  Jurkat cell lysate 100 μL Log in to see 2至3个工作日
$289.00
详细
Cow 非结合性 IHC, WB WB Suggested Anti-TBX19 Antibody Titration:  1.0-1.5ug/ml  Positive Control:  Jurkat cell lysate Human Liver 100 μL Log in to see 2至3个工作日
$249.00
详细
小鼠 非结合性 WB 100 μL Log in to see 11至14个工作日
$522.50
详细
Cow 非结合性 WB 100 μL Log in to see 11至14个工作日
$551.83
详细
Bat 非结合性 IHC, IHC (p), WB 100 μL Log in to see 11至14个工作日
$507.83
详细
非结合性 WB Western blot analysis of extracts of 293T cells, using TBX19 antibody. Western blot analysis of extracts of 293T cells, using TBX19 antibody (ABIN4905379) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 30s. 100 μL Log in to see 11至13个工作日
$366.77
详细
非结合性 ELISA, WB 100 μL Log in to see 2至3个工作日
$446.88
详细
非结合性 IHC, ELISA, WB 100 μL Log in to see 2至3个工作日
$446.88
详细
小鼠 非结合性 WB   100 μL Log in to see 11至14个工作日
$581.17
详细
非结合性 WB   100 μL Log in to see 13至14个工作日
$393.25
详细

更多抗T-Box 19的相互作用对抗体

Human T-Box 19 (TBX19) interaction partners

  1. TBX19 mRNA expression was significantly increased in tumorous tissues compared to that in non-tumorous tissues, and increased TBX19 mRNA expression was associated with positive lymph node metastasis.

  2. Identification of nine new TPIT mutations in a large series of congenital isolated ACTH-deficiency patients.

  3. TPIT is identified as a target autoantigen in 10.5% of patients with lymphocytic hypophysitis.

  4. The coordinate expression of Etv1 with POMC cell differentiation and its interaction with the highly cell-restricted Tpit factor indicate that Etv1 participates in a combinatorial code for pituitary cell-specific gene expression.

  5. Review. Association of 2 mutations with an ACTH deficiency is consistent with the role of tbx19 in differentiation of POMC cells.

  6. TPIT has a role in expression of the pro-opiomelanocortin gene and terminal differentiation of the pituitary corticotroph lineage, and its mutation causes early onset pituitary ACTH deficiency

  7. Tpit, along with NGFI-B and SRC-2, is part of a transcription regulatory complex assembled on the POMC promoter in response to hormonal stimulation.

  8. mutations in the TPIT gene, a T-box factor selectively expressed in developing corticotroph cells, have been found in cases of early-onset isolated ACTH deficiency

  9. TPIT gene mutations is the principal molecular cause of neonatal congenital isolated ACTH deficiency

  10. We report largest series of congenital ACTH deficiency and demonstrate molecular mechanism involves Tpit in majority of cases.

  11. a new mutation (IVS4+1G>A) that affects the first nucleotide of the splice site at the 5' end of the fourth intron in isolated adrenocorticotropic hormone deviciency

  12. Overtransmission of a haplotype GAC at the TBX19 locus was associated with increased angry/hostility scores among suicide attempters.

  13. the M86R TPIT mutation is defining an important surface of the T domain for multiple protein interactions and for transcription

Mouse (Murine) T-Box 19 (TBX19) interaction partners

  1. The coordinate expression of Etv1 with POMC cell differentiation and its interaction with the highly cell-restricted Tpit factor indicate that Etv1 participates in a combinatorial code for pituitary cell-specific gene expression.

  2. Review. Association of 2 mutations with an ACTH deficiency is consistent with the role of tbx19 in differentiation of POMC cells.

  3. TPIT has a role in expression of the pro-opiomelanocortin gene and terminal differentiation of the pituitary corticotroph lineage, and its mutation causes early onset pituitary ACTH deficiency

  4. Tpit has a role as a negative regulator of gonadotroph differentiation in developing mouse

  5. Tpit and NeuroD1 are not essential for early corticotroph commitment. There are different levels of control for commitment of POMC lineages compared to cell survival or to cell-specific transcription of POMC.

  6. the M86R TPIT mutation is defining an important surface of the T domain for multiple protein interactions and for transcription

T-Box 19 (TBX19) 抗原简介

蛋白简介

This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. Mutations in this gene were found in patients with isolated deficiency of pituitary POMC-derived ACTH, suggesting an essential role for this gene in differentiation of the pituitary POMC lineage. ACTH deficiency is characterized by adrenal insufficiency symptoms such as weight loss, lack of appetite (anorexia), weakness, nausea, vomiting, and low blood pressure.

Gene names and symbols associated with anti-T-Box 19 (TBX19) 抗体

  • T-box 19 (TBX19) 抗体
  • T-box 19 (Tbx19) 抗体
  • AU019250 抗体
  • CH-TBXT 抗体
  • D1Ertd754e 抗体
  • dJ747L4.1 抗体
  • TBS19 抗体
  • TBX19 抗体
  • TBXT 抗体
  • Tpit 抗体

Protein level used designations for anti-T-Box 19 (TBX19) 抗体

T-box 19 , T-box transcription factor TBX19-like , T-box factor, pituitary , T-box protein 19 , T-box transcription factor TBX19 , TBS 19 , T-box containing protein , T-box-containing protein TBXT , T-box transcription factor 19

GENE ID SPECIES
699312 Macaca mulatta
748358 Pan troglodytes
100352422 Oryctolagus cuniculus
100403282 Callithrix jacchus
100606186 Nomascus leucogenys
9095 Homo sapiens
395793 Gallus gallus
449029 Canis lupus familiaris
514352 Bos taurus
83993 Mus musculus
304935 Rattus norvegicus
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