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anti-Ganglioside-Induced Differentiation-Associated Protein 1 (GDAP1) Antikörper

GDAP1 encodes a member of the ganglioside-induced differentiation-associated protein family, which may play a role in a signal transduction pathway during neuronal development. Zusätzlich bieten wir Ihnen Ganglioside-Induced Differentiation-Associated Protein 1 Proteine (3) und viele weitere Produktgruppen zu diesem Protein an.

Alle Antikörper anzeigen Gen GeneID UniProt
GDAP1 54332 Q8TB36
GDAP1 14545 O88741
GDAP1 312890  
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Top anti-Ganglioside-Induced Differentiation-Associated Protein 1 Antikörper auf antikoerper-online.de

Showing 10 out of 27 products:

Katalog Nr. Reaktivität Wirt Konjugat Applikation Bilder Menge Anbieter Lieferzeit Preis Details
Human Kaninchen Unkonjugiert WB 50 μg Anmelden zum Anzeigen 6 bis 8 Tage
358,51 €
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Human Kaninchen Unkonjugiert WB 50 μg Anmelden zum Anzeigen 6 bis 8 Tage
358,51 €
Details
Human Maus Unkonjugiert WB GDAP1 polyclonal antibody (A01), Lot # 060613JCS1 Western Blot analysis of GDAP1 expression in HepG2 . Western Blot detection against Immunogen (37.11 KDa) . 50 μL Anmelden zum Anzeigen 8 bis 9 Tage
221,47 €
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Human Kaninchen Unkonjugiert WB   50 μg Anmelden zum Anzeigen 11 bis 14 Tage
653,02 €
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Human Kaninchen Unkonjugiert WB   50 μL Anmelden zum Anzeigen 11 bis 14 Tage
460,95 €
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Human Kaninchen Unkonjugiert WB   50 μL Anmelden zum Anzeigen 7 bis 10 Tage
298,57 €
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Human Kaninchen Unkonjugiert WB   200 μL Anmelden zum Anzeigen 7 bis 8 Tage
510,71 €
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Human Kaninchen Unkonjugiert IHC, WB   100 μL Anmelden zum Anzeigen 12 Days
299,73 €
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Human Kaninchen Alexa Fluor 594 IF (p)   100 μL Anmelden zum Anzeigen 14 bis 17 Tage
366,11 €
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Human Kaninchen Alexa Fluor 350 IF (p)   100 μL Anmelden zum Anzeigen 14 bis 17 Tage
366,11 €
Details

GDAP1 Antikörper nach Reaktivität, Anwendung, Klonalität and Konjugat

Attribute Applikationen Wirt Klonalität
Human , , , ,
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Mouse (Murine) , , , ,

Rat (Rattus) , , , ,

Am meisten referenzierte anti-Ganglioside-Induced Differentiation-Associated Protein 1 Antikörper

  1. Human Polyclonal GDAP1 Primary Antibody für WB,ELISA - ABIN565729 : Cassereau, Chevrollier, Gueguen, Malinge, Letournel, Nicolas, Richard, Ferre, Verny, Dubas, Procaccio, Amati-Bonneau, Bonneau, Reynier: Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K). in Neurogenetics 2009 (PubMed)
    Zeige alle 3 Referenzen für ABIN565729

Weitere Antikörper gegen Ganglioside-Induced Differentiation-Associated Protein 1 Interaktionspartner

Human Ganglioside-Induced Differentiation-Associated Protein 1 (GDAP1) Interaktionspartner

  1. study reports on 2 Charcot-Marie-Tooth (CMT) families in which a newly identified Glu222Lys mutation within the GDAP1 gene segregates both in autosomal dominant and recessive traits

  2. The novelty of our data is the relatively high frequency of SH3TC2 (zeige SH3TC2 Antikörper) and GDAP1 mutations in demyelinating and axonal forms, respectively, of Charcot-Marie-Tooth disease

  3. Results show that JPH1 (zeige JPH1 Antikörper) and GDAP1 share a common pathway and depend on each other; therefore, JPH1 (zeige JPH1 Antikörper) can contribute to the phenotypical consequences of GDAP1 mutations.

  4. GDAP1-associated polyneuropathy caused predominantly a mild and slowly progressive phenotype.

  5. This studies suggest that the pathophysiology of GDAP1-related CMT neuropathies may be associated with abnormal distribution and movement of mitochondria throughout cytoskeleton towards the ER and subplasmalemmal microdomains.

  6. GDAP1 regulates mitochondrial and peroxisomal fission by a similar mechanism.

  7. A novel heterozygous missense mutation (Arg120Gly) in the GDAP1 gene co-segregates with the disease within the pedigree of an Italian Charcot-Marie-Tooth disease type 2 (CMT2) family.

  8. This study suggested that the mutation of GDAP1 cased onion bulb-like formations of schwann cell in peripheral neuropathies.

  9. A French family with Charcot-Marie-Tooth disease is related to simultaneous heterozygous MFN2 (zeige MFN2 Antikörper) and GDAP1 mutations.

  10. Patients of type 4 Charcot-Marie-Tooth disease showed reduced GDAP1 levels, GHS concentration and mitochondrial membrane potential.

Mouse (Murine) Ganglioside-Induced Differentiation-Associated Protein 1 (GDAP1) Interaktionspartner

  1. absence of GDAP1 induces a peripheral neuropathy with loss of motor neurons, mitochondrial defects and abnormal calcium homeostasis.

  2. Members of the GDAP1 family are responsive and protective against stress associated with increased levels of oxidized glutathione.

  3. Cell expression of Gdap1 in the nervous system and pathogenesis of Charcot-Marie-Tooth type 4A disease are reported.

Ganglioside-Induced Differentiation-Associated Protein 1 (GDAP1) Antigen-Profil

Protein Überblick

This gene encodes a member of the ganglioside-induced differentiation-associated protein family, which may play a role in a signal transduction pathway during neuronal development. Mutations in this gene have been associated with various forms of Charcot-Marie-Tooth Disease and neuropathy. Two transcript variants encoding different isoforms and a noncoding variant have been identified for this gene.

Genbezeichner und Symbole assoziert mit GDAP1

  • ganglioside induced differentiation associated protein 1 (GDAP1) Antikörper
  • ganglioside-induced differentiation-associated protein 1 (GDAP1) Antikörper
  • ganglioside-induced differentiation-associated-protein 1 (Gdap1) Antikörper
  • CMT4 Antikörper
  • CMT4A Antikörper
  • CMTRIA Antikörper

Bezeichner auf Proteinebene für GDAP1

ganglioside-induced differentiation-associated protein 1 , Charcot-Marie-Tooth neuropathy 4A , ganglioside differentiation associated protein 1

GENE ID SPEZIES
100172660 Pongo abelii
100050935 Equus caballus
54332 Homo sapiens
420191 Gallus gallus
487002 Canis lupus familiaris
100157012 Sus scrofa
613472 Bos taurus
14545 Mus musculus
312890 Rattus norvegicus
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