Anoctamin 5 (ANO5) ELISA Kits

ANO5 encodes a member of the anoctamin family of transmembrane proteins. Zusätzlich bieten wir Ihnen Anoctamin 5 Antikörper (23) und Anoctamin 5 Proteine (5) und viele weitere Produktgruppen zu diesem Protein an.

list all ELISA KIts Gen GeneID UniProt
Anti-Human ANO5 ANO5 203859 Q75V66
Anti-Maus ANO5 ANO5 233246 Q75UR0
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Weitere ELISA Kits für Anoctamin 5 Interaktionspartner

Human Anoctamin 5 (ANO5) Interaktionspartner

  1. Asymptomatic, sometimes mild hyperCKemia or exercise intolerance is a presentation of ANO5-related myopathy.

  2. Here we show that Ano5-deficient mice have reduced capacity to repair the sarcolemma following laser-induced damage, exhibit delayed regeneration after cardiotoxin injury and suffer from defective myoblast fusion necessary for the proper repair and regeneration of multinucleated myotubes. these data suggest that ANO5 plays an important role in sarcolemmal membrane dynamics.

  3. Study screened the ANO5 gene in 786 myopathic patients and 52 controls by combining NGS and Sanger sequencing. In the cohort of patients, thirty-three are homozygous or compound heterozygous for causative mutations in ANO5

  4. supervised aerobic exercise training is safe and effective in improving oxidative capacity and muscle function in patients with anoctamin 5 deficiency

  5. The present report describes an association between LGMD2L consequent upon mutation in ANO5 and macular dystrophy in one affected person.

  6. Dilated cardiomyopathy is associated with mutations in the ANO5 gene.

  7. ANO5 mutations can be associated with amyloid deposition in muscle

  8. A high prevalence of ANO5 deficiency was found among patients with unclassified recessive limb girdle muscular dystrophy 2

  9. a diagnosis of ANO5 causing Muscular Dystrophy, Limb-Girdle, Type 2L, in 16% of the families (11/68) in a well-defined limb girdle muscular dystrophy cohort in the Netherlands

  10. investigated the prevalence and spectrum of ANO5 gene mutations and related clinical phenotypes; study confirmed that ANO5 gene mutations are responsible for about one fourth of cases of undiagnosed muscular dystrophy in the population studied

Mouse (Murine) Anoctamin 5 (ANO5) Interaktionspartner

  1. Here we show that Ano5-deficient mice have reduced capacity to repair the sarcolemma following laser-induced damage, exhibit delayed regeneration after cardiotoxin injury and suffer from defective myoblast fusion necessary for the proper repair and regeneration of multinucleated myotubes. these data suggest that ANO5 plays an important role in sarcolemmal membrane dynamics.

  2. TMEM16E(-/-) sperm showed no apparent defect in morphology, beating, mitochondrial function, capacitation, or binding to zona pellucida. However, they showed reduced motility and inefficient fertilization of cumulus-free but zona-intact eggs in vitro.

  3. Ano5 mRNA and protein are widely expressed in the esophagus, stomach, duodenum, colon and rectum but Ano5 immunoreactivity are only detected in the mucosal layer, except for the muscular layer of the upper esophagus, which consists of skeletal muscle.

  4. characterized the complete cDNA sequence and genomic organization of the mouse GDD1 gene

  5. These observations suggest diverse cellular role(s) of GDD1 in the development of musculoskeletal system.

Anoctamin 5 (ANO5) Antigen-Profil

Beschreibung des Gens

This gene encodes a member of the anoctamin family of transmembrane proteins. The encoded protein is likely a calcium activated chloride channel. Mutations in this gene have been associated with gnathodiaphyseal dysplasia. Alternatively spliced transcript variants have been described.

Genbezeichner und Symbole assoziert mit Anoctamin 5 (ANO5) ELISA Kits

  • anoctamin 5 L homeolog (ano5.L) Antikörper
  • anoctamin 5 (ANO5) Antikörper
  • anoctamin 5a (ano5a) Antikörper
  • anoctamin 5 (ano5) Antikörper
  • anoctamin 5 (Ano5) Antikörper
  • 9330162L24 Antikörper
  • ano5 Antikörper
  • Gdd1 Antikörper
  • LGMD2L Antikörper
  • MGC82557 Antikörper
  • si:dkey-261m9.4 Antikörper
  • Tmem16e Antikörper

Bezeichner auf Proteinebene für Anoctamin 5 (ANO5) ELISA Kits

anoctamin 5 , transmembrane protein 16E , anoctamin-5 , anoctamin-5-like , tmem16ea , gnathodiaphyseal dysplasia 1 protein , integral membrane protein GDD1 , limb girdle muscular dystrophy 2L (autosomal recessive) , gnathodiaphyseal dysplasia 1 protein homolog

GENE ID SPEZIES
446645 Xenopus laevis
485416 Canis lupus familiaris
100072055 Equus caballus
100140158 Bos taurus
100340377 Oryctolagus cuniculus
100389212 Callithrix jacchus
100459066 Pongo abelii
100484835 Ailuropoda melanoleuca
100534737 Danio rerio
100549161 Meleagris gallopavo
100567373 Anolis carolinensis
100587082 Nomascus leucogenys
100617099 Monodelphis domestica
203859 Homo sapiens
233246 Mus musculus
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