anti-Forkhead Box N1 (FOXN1) 抗体

The protein encoded by FOXN1 is part of the forkhead family or 'winged-helix' transcription factors that are important in developmental processes, immune system regulation, metabolism, cancer and aging. 再加上,我们可以发FOXN1 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
FOXN1 8456 O15353
FOXN1 15218 Q61575
FOXN1 287469  
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antibodies-online.cn销售最多的anti-FOXN1 抗体

Showing 10 out of 82 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-FOXN1 Antibody Titration: 5.0ug/ml ELISA Titer: 1:1562500 Positive Control: Raji cell lysate FOXN1 is supported by BioGPS gene expression data to be expressed in Raji 100 μL Log in to see 2至3个工作日
$229.00
详细
非结合性 EIA, FACS, WB Flow cytometric analysis of A549 cells using FOXN1 Antibody (Center) Cat.-No AP51716PU-N (right histogram) compared to a negative control cell (left histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis. Western blot analysis of FOXN1 Antibody (Center) in A549,NCI-H460 cell line lysates (35ug/lane). This demonstrates the FOXN1 antibody detected the FOXN1 protein (arrow). 0.4 mL Log in to see 6至8个工作日
$390.50
详细
山羊 非结合性 IHC, ELISA, WB ABIN185069 (20µg/ml) staining of paraffin embedded Human Thymus Medulla. Steamed antigen retrieval with citrate buffer pH 6, AP-staining. 100 μg Log in to see 6至7个工作日
$358.02
详细
非结合性 WB 100 μg Log in to see 7至9个工作日
$493.17
详细
非结合性 FACS, WB FOXN1 Antibody (Center) (ABIN655992) western blot analysis in A549,NCI-H460 cell line lysates (35 µg/lane). This demonstrates the FOXN1 antibody detected the FOXN1 protein (arrow). 400 μL Log in to see 10至11个工作日
$324.50
详细
山羊 非结合性 IHC (p), IHC, ELISA Immunohistochemistry: FOXN1 Antibody [ABIN250004] - B100-1302 (20?g/ml) staining of paraffin embedded Human Thymus Medulla. Steamed antigen retrieval with citrate buffer pH 6, AP-staining. 0.1 mg Log in to see 7至9个工作日
$485.88
详细
非结合性 IF (p), IHC (p), WB Formalin-fixed and paraffin embedded rat colon labeled with Anti-FOXN1 Polyclonal Antibody, Unconjugated (ABIN1387592) at 1:200 followed by conjugation to the secondary antibody and DAB staining Formalin-fixed and paraffin embedded mouse spleen labeled with Anti-FOXN1 Polyclonal Antibody, Unconjugated (ABIN1387592) at 1:200 followed by conjugation to the secondary antibody and DAB staining 100 μL Log in to see 3至7个工作日
$318.45
详细
非结合性 WB WB Image FOXN1 antibody [C3], C-term detects FOXN1 protein by western blot analysis. Various whole cell extracts (30 μg) were separated by 7.5% SDS-PAGE, and the membrane was blotted with FOXN1 antibody [C3], C-term , diluted at 1:500. WB Image FOXN1 antibody [C3], C-term detects FOXN1 protein by western blot analysis. Various whole cell extracts (30 μg) were separated by 7.5% SDS-PAGE, and the membrane was blotted with FOXN1 antibody [C3], C-term , diluted at 1:500. 100 μL Log in to see 1至2个工作日
$358.60
详细
非结合性 IHC (p), WB Human Uterus: Formalin-Fixed, Paraffin-Embedded (FFPE) Sample (30 ug of whole cell lysate). A: Raji. 7.5% SDS PAGE. FOXN1 antibody diluted at 1:1000. 50 μL Log in to see 6至8个工作日
$368.50
详细
山羊 非结合性 EIA, IHC (p) 50 μg Log in to see 6至8个工作日
$368.50
详细

通过反应活性、应用领域、克隆类型和共轭标记 FOXN1 抗体

特性 应用范围 宿主 克隆类型 标记
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引用最多的anti-FOXN1 抗体

  1. Human Polyclonal FOXN1 Primary Antibody for IHC (p), IHC - ABIN250004 : Schlake, Schorpp, Maul-Pavicic, Malashenko, Boehm: Forkhead/winged-helix transcription factor Whn regulates hair keratin gene expression: molecular analysis of the nude skin phenotype. in Developmental dynamics : an official publication of the American Association of Anatomists 2000 (PubMed)

更多抗FOXN1的相互作用对抗体

Zebrafish Forkhead Box N1 (FOXN1) interaction partners

  1. the foxn1-mcm2 (显示 MCM2 抗体) axis plays a central role in the genetic regulatory network controlling thymus development in zebrafish

  2. zebrafish orthologue (whnb) of the mouse nude gene is expressed in the epithelial compartment of the embryonic thymic rudiment

  3. an evolutionarily conserved role of BMP signaling in the maintenance of Foxn1 expression.

Human Forkhead Box N1 (FOXN1) interaction partners

  1. FOXN1 founder Italian mutation identified in an indian newborn with severe combined immunodeficiency (显示 PRKDC 抗体).

  2. Whole-exome sequencing in a South American coh (显示 RARB 抗体)ort links ALDH1A3, FOXN1 and RARB/retinoic acid regulation pathways to autism s (显示 ALDH1A3 抗体)pectrum disorders.

  3. Identification of a unique mutation in FOXN1 that led to severe combined immunodeficiency (显示 PRKDC 抗体) in a female infant is reported.

  4. These results show that miR (显示 MLXIP 抗体)-18b and miR (显示 MLXIP 抗体)-518b are upstream controllers of FOXN1-directed epithelial lineage development.

  5. The retinoid-related orphan receptor (显示 NR1D2 抗体) RORalpha promotes keratinocyte differentiation via FOXN1.

  6. This is the first description of leucoderma occurring in a patient with Foxn1 deficiency, as well as the first report of this pigment abnormality following thymus transplantation.

  7. results show that FOXN1 is crucial for in utero T cell development, but not for B and NK cell differentiation

  8. role of FOXN1 in immunological disorders characterized by abnormal T-cell development or abnormal T-cell regulatory homeostasis [Review]

  9. study uncovered a positive regulatory loop between FGFR3 (显示 FGFR3 抗体) and FOXN1 that underlies a benign versus malignant skin tumor phenotype

  10. Mutation of the FOXN1 gene is associated with congenital severe combined immunodeficiency (显示 PRKDC 抗体) associated with alopecia

Mouse (Murine) Forkhead Box N1 (FOXN1) interaction partners

  1. MicroRNA-205 maintains T cell development following stress by regulating Foxn1 (显示 FOXN2 抗体) and its two regulated targets, stem cell factor (显示 KITLG 抗体) and ccl25 (显示 CCL25 抗体), following stress.

  2. this study identified Bmp4 (显示 BMP4 抗体) as a significant factor for improved maintenance of Foxn1 (显示 FOXN2 抗体) expression, promotion of thymic epithelial progenitor populations self-renewal and immature epithelial cell differentiation and survival

  3. results show that Foxn1 (显示 FOXN2 抗体), and alleles under its control, are expressed in the pre-meiotic male germline, revealing a new tool for germline targeting of genes, and raising important concerns for gender selection when using Foxn1 (显示 FOXN2 抗体) regulatory elements.

  4. this study shows that critical events in thymic lympho-stromal cross-talk and T cell selection are regulated by Foxn1 (显示 FOXN2 抗体)

  5. sphingolipids and fatty acids associated with a decrease in glycerolipids suggest that the lipidome in mice skin is regulated by the Foxn1 (显示 FOXN2 抗体) gene

  6. Foxn1 (显示 FOXN2 抗体) transcription factor regulates wound healing of skin through promoting epithelial-mesenchymal transition.

  7. early differentiation and maturation of cortical and medullary thymic epithelial cells coincides with precise sub-lineage-specific regulation of Foxn1 (显示 FOXN2 抗体) expression levels.

  8. Chromatin immunoprecipitation assay using RarB (显示 RARB 抗体) as the immunoprecipitation target suggests retinoic acid regulation of Aldh1a3 (显示 ALDH1A3 抗体) and Foxn1 (显示 FOXN2 抗体) in mice.

  9. The maturation and distribution of thymic epithelial cells in the Foxn1 (显示 FOXN2 抗体)(-/-) thymic rudiment and the thymopoiesis of this newly developed rudiment, were examined.

  10. Expression of FoxN1 (显示 FOXN2 抗体) in early life adversely influence immature epithelial cells T and B cell, and skin epithelial development.

FOXN1 抗原简介

蛋白简介

The protein encoded by this gene is part of the forkhead family or 'winged-helix' transcription factors that are important in developmental processes, immune system regulation, metabolism, cancer and aging. This gene family has over 100 members, subdivided into classes (A-Q) based on phylogeny. The encoded protein is proposed to regulate development of the thymus and differentiation of keratinocytes. Mutations in this gene cause severe primary T-cell immunodeficiency and congenital alopecia. In mouse mutations of this gene underlie the phenotype of the nude mouse, which has been widely used as a model system in oncology, immunology, dermatology, and transplantation studies. In humans mutations in this gene have been correlated with T-cell immunodeficiency, the skin disorder congenital alopecia, and nail dystrophy. Alternative splicing results in multiple transcript variants that encode different protein isoforms.

Gene names and symbols associated with anti-Forkhead Box N1 (FOXN1) 抗体

  • forkhead box N1 (FOXN1) 抗体
  • forkhead box N1 (foxn1) 抗体
  • forkhead box N1 (foxN1) 抗体
  • forkhead box protein N1 (LOC100125524) 抗体
  • forkhead box N1 (Foxn1) 抗体
  • D11Bhm185e 抗体
  • Fkh19 抗体
  • FKHL20 抗体
  • foxN 抗体
  • foxn1 抗体
  • HFH-11 抗体
  • Hfh11 抗体
  • nu 抗体
  • nude 抗体
  • Rnu 抗体
  • RONU 抗体
  • Whn 抗体
  • whnb 抗体

Protein level used designations for anti-Forkhead Box N1 (FOXN1) 抗体

forkhead box protein N1 , forkhead box N1 , forkhead box N protein , forkhead box protein N1-like , transcription factor Forkhead box protein N1 , Rowett nude , winged helix nude , winged-helix nude , winged-helix transcription factor nude , HNF-3/forkhead homolog 11 , hepatocyte nuclear factor 3 forkhead homolog 11

GENE ID SPECIES
417570 Gallus gallus
100059109 Equus caballus
266748 Danio rerio
468381 Pan troglodytes
708926 Macaca mulatta
100024620 Monodelphis domestica
100303472 Saccoglossus kowalevskii
100410086 Callithrix jacchus
100467385 Ailuropoda melanoleuca
100601006 Nomascus leucogenys
100125524 Oryzias latipes
8456 Homo sapiens
491168 Canis lupus familiaris
516724 Bos taurus
15218 Mus musculus
287469 Rattus norvegicus
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