anti-Chromosome 5 Open Reading Frame 42 (C5ORF42) Antikörper

The protein encoded by C5ORF42 has putative coiled-coil domains and may be a transmembrane protein.

Alle Antikörper anzeigen Gen GeneID UniProt
C5ORF42 65250 Q9H799
C5ORF42    
C5ORF42    
Direkt bei antikoerper-online bestellen
  • +1 877 302 8632
  • +1 888 205 9894 (toll-free)
  • Online bestellen
  • orders@antikoerper-online.de

Top anti-C5ORF42 Antikörper auf antikoerper-online.de

Showing 10 out of 16 products:

Katalog Nr. Reaktivität Wirt Konjugat Applikation Bilder Menge Lieferzeit Preis Details
Human Kaninchen Alexa Fluor 594 IF (p)   100 μL 14 bis 21 Tage
$416.90
Details
Human Kaninchen Alexa Fluor 350 IF (p)   100 μL 3 bis 7 Tage
$416.90
Details
Human Kaninchen Alexa Fluor 488 IF (p)   100 μL 3 bis 7 Tage
$416.90
Details
Human Kaninchen Alexa Fluor 555 IF (p)   100 μL 3 bis 7 Tage
$416.90
Details
Human Kaninchen Alexa Fluor 647 IF (p)   100 μL 3 bis 7 Tage
$416.90
Details
Human Kaninchen Cy3 IF (p)   100 μL 3 bis 7 Tage
$416.90
Details
Human Kaninchen Cy5 IF (p)   100 μL 3 bis 7 Tage
$416.90
Details
Human Kaninchen Cy5.5 IF (p)   100 μL 3 bis 7 Tage
$416.90
Details
Human Kaninchen Cy7 IF (p)   100 μL 3 bis 7 Tage
$416.90
Details
Human Kaninchen FITC IF (p)   100 μL 3 bis 7 Tage
$416.90
Details

Am meisten referenzierte anti-C5ORF42 Antikörper

  1. Human Polyclonal C5ORF42 Primary Antibody für ICC, IF - ABIN4286500 : Hong, Joo, Park, Seo, Kim, Shin, Cheong, Lee, Kim: Extraciliary roles of the ciliopathy protein JBTS17 in mitosis and neurogenesis. in Annals of neurology 2019 (PubMed)

Weitere Antikörper gegen C5ORF42 Interaktionspartner

Human Chromosome 5 Open Reading Frame 42 (C5ORF42) Interaktionspartner

  1. Seven novel germline recessive mutations in CPLANE1, including missense, nonsense, frameshift and canonical splice site variants, were identified in OFD6 patients.

  2. In C5orf42-mutant Joubert syndrome patients, the infratentorial magnetic resonance images showed normal or minimally thickened and minimally elongated superior cerebellar peduncles, normal or minimally deepened interpeduncular fossa, and mild vermian hypoplasia.

  3. C5orf42 is one of the causative genes for OFDVI.

  4. C5orf42 mutation is associated with Oral-facial-digital syndrome type VI.

  5. We identified causal C5orf42 mutations in 9/11 families meeting OFD VI diagnostic criteria, but no mutation in individuals with partly overlapping features.

  6. Exome sequencing revealed a likely pathogenic mutation in three novel candidate MKS disease genes-C5orf42, EVC2 and SEC8 (also known as EXOC4), which encodes an exocyst protein with an established role in ciliogenesis

  7. C5orf42 and KIAA1377 gene synergistically play a role as susceptibility genes for monomelic amyotrophy.

  8. The data suggested that mutations in C5ORF42 explain a large percentage of French Canadian individuals with Joubert syndrome.

C5ORF42 Antigen-Profil

Protein Überblick

The protein encoded by this gene has putative coiled-coil domains and may be a transmembrane protein. Defects in this gene are a cause of Joubert syndrome (JBTS).

Genbezeichner und Symbole assoziert mit C5ORF42

  • chromosome 5 open reading frame 42 (C5orf42) Antikörper
  • JBTS17 Antikörper

Bezeichner auf Proteinebene für C5ORF42

Transmembrane protein ENSP00000382582 , uncharacterized protein C5orf42

GENE ID SPEZIES
65250 Homo sapiens
Ausgewählte Anbieter für anti-C5ORF42 (C5ORF42) Antikörper
Haben Sie etwas anderes gesucht?