anti-Ankyrin Repeat Domain 11 (ANKRD11) Antikörper

This locus encodes an ankryin repeat domain-containing protein.

Alle Antikörper anzeigen Gen GeneID UniProt
ANKRD11 29123 Q6UB99
ANKRD11 77087  
ANKRD11 365023  
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Top anti-ANKRD11 Antikörper auf antikoerper-online.de

Showing 10 out of 31 products:

Katalog Nr. Reaktivität Wirt Konjugat Applikation Bilder Menge Lieferzeit Preis Details
Rind (Kuh) Kaninchen Unkonjugiert IHC, WB Human kidney WB Suggested Anti-ANKRD11 Antibody Titration: 1.25ug/ml Positive Control: Human Placenta 100 μL 2 bis 3 Tage
$229.00
Details
Fledermaus Kaninchen Unkonjugiert IHC, IHC (p), WB 100 μL 11 bis 14 Tage
$493.17
Details
Human Kaninchen Unkonjugiert IHC, WB ANKRD11 antibody was used for immunohistochemistry at a concentration of 4-8 ug/ml to stain Epithelial cells of renal tubule (arrows) in Human Kidney. Magnification is at 400X ANKRD11 antibody used at 1.25 ug/ml to detect target protein. 100 μg 9 bis 11 Tage
$369.29
Details
Hund Kaninchen Unkonjugiert IHC, ELISA, WB 100 μL 2 bis 3 Tage
$446.88
Details
Human Kaninchen Unkonjugiert IF (p), IHC (p), WB Antigen: 0.2 µg/100 µL Primary: Antiserum, 1:500, 1:1000, 1:2000, 1:4000, 1:8000, 1:16000, 1:32000; Secondary: HRP conjugated Goat-Anti-Rabbit IgG at 1: 5000; TMB staining; Read the data in MicroplateReader by 450 Antigen: 0.2ug/100ul, Primary: Antiserum, 1:500, 1:1000, 1:2000, 1:4000, 1:8000, 1:16000, 1:32000, Secondary: HRP conjugated Goat-Anti-Rabbit IgG at 1: 5000, TMB staining, Read the data in MicroplateReader by 450nm 100 μL 3 bis 7 Tage
$317.90
Details
Human Maus Unkonjugiert DB, WB   100 μg 11 bis 14 Tage
$837.83
Details
Human Kaninchen Unkonjugiert IHC (p), WB Immunohistochemical staining (Formalin-fixed paraffin-embedded sections) of human kidney with ANKRD11 polyclonal antibody at 4-8 ug/mL working concentration. Western Blot analysis of human placenta tissue lysate with ANKRD11 polyclonal antibody at 1.25 ug/mL working concentration. 100 μL 11 bis 12 Tage
$356.00
Details
Human Kaninchen Cy7 IF (p)   100 μL 14 bis 21 Tage
$416.90
Details
Human Kaninchen Cy5 IF (p)   100 μL 14 bis 21 Tage
$416.90
Details
Human Kaninchen Cy3 IF (p)   100 μL 14 bis 21 Tage
$416.90
Details

Weitere Antikörper gegen ANKRD11 Interaktionspartner

Human Ankyrin Repeat Domain 11 (ANKRD11) Interaktionspartner

  1. Novel ANKRD11 gene mutation in an individual with a mild phenotype of KBG syndrome associated to a GEFS+ phenotypic spectrum.

  2. ANKRD11 variants cause KBG syndrome and Coffin-Siris-like syndrome.

  3. ANKRD11 variants cause variable clinical features associated with KBG syndrome and Coffin-Siris-like syndrome.

  4. exome sequencing identified a novel de novo heterozygous single base pair duplication (c.6015dupA) in ANKRD11, which is predicted to lead to a premature stop codon and loss of function in ANKRD11, thereby implicating it as contributing to the molecular diagnosis of KBG syndrome.

  5. Here we report a large series of 39 patients with KBG syndrome; these patients harbored ANKRD11 mutations (20 cases) or deletions (19 cases). All the mutations were found by targeted molecular analysis on patients with clinical features suggestive of KBG.

  6. Twelve novel cases of haploinsufficiency for ANKRD11-flanking genes make the difference between KBG and 16q24.3 microdeletion syndromes.

  7. These findings point out the importance of screening ANKRD11 in young CdLS patients who were found to be negative for mutations in the five known CdLS genes.

  8. Further delineation of the KBG syndrome phenotype on large patients cohort caused by ANKRD11 aberrations has been presented.

  9. we conclude that severe short stature, intellectual disability, and macrodontia are the main characteristics in KBG syndrome related to ANKRD11 mutation

  10. ANKRD11 C-terminus plays an important role in regulating the abundance of the protein, and a disturbance of the protein abundance due to the mutations leads to KBG syndrome.

  11. AIB1, AIB1-delta4 and ANCO1 are important determinants of endocrine and growth factor responsiveness in breast cancer.

  12. The complete neurological and psychiatric features observed in two patients with KBG syndrome due to ANKRD11 mutations, are reported.

  13. Partial deletion of ANKRD11 results in the KBG phenotype distinct from the 16q24.3 microdeletion syndrome.

  14. aberrant DNA methylation of three CpGs in a 19 bp region within the ANKRD11 promoter may be responsible for its down-regulation in breast cancer.

  15. Mutations in ANKRD11 cause KBG syndrome and outline a fundamental role of ANKRD11 in craniofacial, dental, skeletal, and central nervous system development and function.

  16. ANKRD11 is a candidate gene for autism and variable cognitive impairment in the novel 16q24.3 microdeletion syndrome.

  17. Together, these results indicate that the transcriptional potential of ANCO-1 may be modulated by a combination of repression and activation signals.

  18. ANKRD11 has a role as a p53 coactivator and may be involved in a regulatory feedback loop with p53

Mouse (Murine) Ankyrin Repeat Domain 11 (ANKRD11) Interaktionspartner

  1. Ankrd11 knockdown delayed radial migration of cortical neurons. ANKRD11-deficient neurons displayed markedly reduced dendrite growth and branching as well as abnormal dendritic spine morphology. Ankrd11 knockdown suppressed acetylation of epigenetic molecules such as p53 and Histone H3. Furthermore, the mRNA levels of Trkb, Bdnf, and neurite growth-related genes were downregulated in ANKRD11-deficient cortical neurons.

  2. ANKRD11 C-terminus plays an important role in regulating the abundance of the protein, and a disturbance of the protein abundance due to the mutations leads to KBG syndrome.

  3. A Glu->Lys missense mutation in a highly conserved region causes osteopenia and craniofacial abnormalities. Homozygosity causes embryo death. Ankrd11 is a genetic regular of bone homeostasis.

ANKRD11 Antigen-Profil

Protein Überblick

This locus encodes an ankryin repeat domain-containing protein. The encoded protein inhibits ligand-dependent activation of transcription. Mutations in this gene have been associated with KBG syndrome, which is characterized by macrodontia, distinctive craniofacial features, short stature, skeletal anomalies, global developmental delay, seizures and intellectual disability. Alternatively spliced transcript variants have been described. Related pseudogenes exist on chromosomes 2 and X.

Genbezeichner und Symbole assoziert mit ANKRD11

  • ankyrin repeat domain 11 (ANKRD11) Antikörper
  • ankyrin repeat domain 11 (Ankrd11) Antikörper
  • ankyrin repeat domain 11 L homeolog (ankrd11.L) Antikörper
  • ankyrin repeat domain 11 (ankrd11) Antikörper
  • 2410104C19Rik Antikörper
  • 3010027A04Rik Antikörper
  • 6330578C09Rik Antikörper
  • 9530048I21Rik Antikörper
  • AA930108 Antikörper
  • ANCO-1 Antikörper
  • ANCO1 Antikörper
  • ANKRD11 Antikörper
  • Gm176 Antikörper
  • LZ16 Antikörper
  • T13 Antikörper
  • wu:fc59e05 Antikörper
  • wu:fi04c06 Antikörper
  • Yod Antikörper

Bezeichner auf Proteinebene für ANKRD11

ankyrin repeat domain-containing protein 11 , ankyrin repeat-containing cofactor 1 , nasopharyngeal carcinoma susceptibility protein , ankyrin repeat domain 11 , ankyrin repeat domain-containing protein 11-like , fc59e05 , fi04c06

GENE ID SPEZIES
29123 Homo sapiens
77087 Mus musculus
365023 Rattus norvegicus
415845 Gallus gallus
443986 Xenopus laevis
468078 Pan troglodytes
489658 Canis lupus familiaris
532856 Bos taurus
698722 Macaca mulatta
100050107 Equus caballus
100431329 Pongo abelii
100077260 Ornithorhynchus anatinus
100223787 Taeniopygia guttata
100485818 Xenopus (Silurana) tropicalis
100727156 Cavia porcellus
327352 Danio rerio
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