Gigaxonin Proteine (GAN)

GAN encodes a member of the cytoskeletal BTB/kelch (Broad-Complex, Tramtrack and Bric a brac) repeat family. Zusätzlich bieten wir Ihnen GAN Antikörper (41) und GAN Kits (8) und viele weitere Produktgruppen zu diesem Protein an.

alle Proteine anzeigen Gen GeneID UniProt
GAN 209239 Q8CA72
Ratte GAN GAN 307893  
GAN 8139 Q9H2C0
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Showing 4 out of 5 products:

Katalog Nr. Origin Quelle Konjugat Bilder Menge Anbieter Lieferzeit Preis Details
Insektenzellen Maus His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Anmelden zum Anzeigen 56 Days
7.380,00 €
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Insektenzellen Human His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Anmelden zum Anzeigen 56 Days
7.380,00 €
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HOST_Wheat germ Human GST tag 10 μg Anmelden zum Anzeigen 7 bis 8 Tage
345,60 €
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HOST_Escherichia coli (E. coli) Human S tag,His tag   100 μg Anmelden zum Anzeigen 13 bis 17 Tage
609,52 €
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GAN Proteine nach Spezies und Herkunft

Origin Exprimiert in Konjugat
Mouse (Murine)

Human , ,
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Weitere Proteine zu Gigaxonin (GAN) Interaktionspartnern

Mouse (Murine) Gigaxonin (GAN) Interaktionspartner

  1. We demonstrate that gigaxonin is crucial for ubiquitin-proteasomal degradation of neuronal Intermediate filaments. Moreover,Intermediate filaments accumulation impairs mitochondrial motility and is associated with metabolic and oxidative stress

  2. gigaxonin is a major factor in the degradation of cytoskeletal intermediate filaments

  3. GAN variants are identified in brain sections of mutant mice with giant axonal neuropathy.

  4. results identify gigaxonin as a ubiquitin scaffolding protein that controls MAP1B (zeige MAP1B Proteine)-LC degradation, and provide insight into the molecular mechanisms underlying human neurodegenerative disorders

  5. Disruption of gigaxonin results in an impaired ubiquitin-proteasome system leading to a substantial accumulation of toxic microtubule-associated protein (zeige SPAG5 Proteine) MAP8 (zeige MAP1S Proteine) in the null mutants.

  6. At 6 months of age the Gigaxonin-knockout(Deltaexon1;Deltaexon1) mice exhibit a modest hind limb muscle atrophy, a 10% decrease of muscle innervation and a 27% axonal loss in the L5 ventral roots.

Human Gigaxonin (GAN) Interaktionspartner

  1. We believe that molecular and functional investigation of gigaxonin mutations including the exon 8 polymorphism could lead to an improved understanding of the relationship between GAN and cancer

  2. A novel sequence alteration in the gene GAN, c.103G > T, was identified as most likely the underlying cause for a sensory-motor axonal neuropathy in a large consanguineous family presenting as Charcot-Marie-Tooth disease type 2.

  3. The disease is caused by GAN gene mutations on chromosome 16q24.1. To determine clinical and genetic results in Turkish patients with GAN.

  4. This study showed that The instability of Gigaxonin causes Giant Axonal Neuropathy.

  5. A novel missense mutation in four siblings born to consanguineous parents of Arab origin with clinical and molecular features compatible with giant axonal neuropathy.

  6. gigaxonin is a major factor in the degradation of cytoskeletal intermediate filaments

  7. No GAN variant is identified in DNA obtained from well-characterized cases of human neuronal intermediate filament inclusion disease (frontotemporal dementia).

  8. Gigaxonin interacts with tubulin folding cofactor B and controls its degradation through the ubiquitin-proteasome pathway.

  9. Ubiquitin-proteasome system shown to be responsible for neurodegeneration occurring in GAN-null neurons and plays crucial roles in cytoskeletal functions and dynamics.

  10. 3 new mutants were found in patients with giant axonal neuropathy: an intronic mutation near the splice donor site of intron 2 & a missense mutation in exon 3 (I182N), & 2 identical deletion alleles.

GAN Protein Überblick

Protein Überblick

This gene encodes a member of the cytoskeletal BTB/kelch (Broad-Complex, Tramtrack and Bric a brac) repeat family. The encoded protein plays a role in neurofilament architecture and is involved in mediating the ubiquitination and degradation of some proteins. Defects in this gene are a cause of giant axonal neuropathy (GAN).

Genbezeichner und Symbole assoziert mit Gigaxonin Proteine (GAN)

  • gigaxonin (gan)
  • gigaxonin (GAN)
  • giant axonal neuropathy (gigaxonin) (GAN)
  • giant axonal neuropathy (Gan)
  • gigaxonin (Gan)
  • A330045G18 Protein
  • GAN Protein
  • GAN1 Protein
  • gigaxonin Protein
  • KLHL16 Protein
  • MGC81691 Protein

Bezeichner auf Proteinebene für Gigaxonin Proteine (GAN)

gigaxonin , giant axonal neuropathy , giant axonal neuropathy (gigaxonin) , kelch-like family member 16 , kelch-like protein 16

GENE ID SPEZIES
447405 Xenopus laevis
549284 Xenopus (Silurana) tropicalis
713996 Macaca mulatta
100027517 Monodelphis domestica
100339638 Oryctolagus cuniculus
100388790 Callithrix jacchus
100453030 Pongo abelii
100484003 Ailuropoda melanoleuca
100549375 Meleagris gallopavo
100586857 Nomascus leucogenys
430553 Gallus gallus
468044 Pan troglodytes
489694 Canis lupus familiaris
100069891 Equus caballus
209239 Mus musculus
307893 Rattus norvegicus
8139 Homo sapiens
100518489 Sus scrofa
521175 Bos taurus
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