Tetratricopeptide Repeat Domain Protein 21B (TTC21B)

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THM1

Tetratricopeptide Repeat Domain Protein 21B (TTC21B)
Aln mutant cilia have bulb-like structures at their tips in which intraflagellar transport (IFT) proteins such as Ift88 are sequestered, characteristic of Chlamydomonas reinhardtii and Caenorhabditis elegans retrograde IFT mutants. Ttc21b, in mouse intermedullary collecting duct cells expressing an Ift88-enhanced yellow fluorescent protein fusion recapitulated the aln-mutant cilial phenotype, and live imaging of these cells revealed impaired retrograde intraflagellar transport. In contrast to previously described IFT mutants, Smoothened and full-length glioblastoma (GLI) proteins localize to aln-mutant cilia. Specifically, the aln mutation uncouples the roles of anterograde and retrograde transport in Sonic hedgehog signaling, suggesting that anterograde IFT is required for GLI activation and that retrograde IFT modulates this event.

Organism species: Homo sapiens (Human)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Tetratricopeptide Repeat Domain Protein 21B (TTC21B) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Tetratricopeptide Repeat Domain Protein 21B (TTC21B) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Tetratricopeptide Repeat Domain Protein 21B (TTC21B) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Tetratricopeptide Repeat Domain Protein 21B (TTC21B) CLIA Kit Customized Service Offer
n/a ELISA Kit for Tetratricopeptide Repeat Domain Protein 21B (TTC21B) ELISA Kit Customized Service Offer

Organism species: Mus musculus (Mouse)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Tetratricopeptide Repeat Domain Protein 21B (TTC21B) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Tetratricopeptide Repeat Domain Protein 21B (TTC21B) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Tetratricopeptide Repeat Domain Protein 21B (TTC21B) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Tetratricopeptide Repeat Domain Protein 21B (TTC21B) CLIA Kit Customized Service Offer
n/a ELISA Kit for Tetratricopeptide Repeat Domain Protein 21B (TTC21B) ELISA Kit Customized Service Offer

Organism species: Rattus norvegicus (Rat)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Tetratricopeptide Repeat Domain Protein 21B (TTC21B) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Tetratricopeptide Repeat Domain Protein 21B (TTC21B) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Tetratricopeptide Repeat Domain Protein 21B (TTC21B) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Tetratricopeptide Repeat Domain Protein 21B (TTC21B) CLIA Kit Customized Service Offer
n/a ELISA Kit for Tetratricopeptide Repeat Domain Protein 21B (TTC21B) ELISA Kit Customized Service Offer
  1. "Neuroblastoma oligo-capping cDNA project: toward the understanding of the genesis and biology of neuroblastoma."Cancer Lett. 197:63-68(2003) [PubMed] [Europe PMC] [Abstract]
  2. "Generation and annotation of the DNA sequences of human chromosomes 2 and 4." Nature 434:724-731(2005) [PubMed] [Europe PMC] [Abstract]
  3. "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]
  4. "Complete sequencing and characterization of 21,243 full-length human cDNAs." Nat. Genet. 36:40-45(2004) [PubMed] [Europe PMC] [Abstract]
  5. "Characterization of size-fractionated cDNA libraries generated by the in vitro recombination-assisted method."DNA Res. 9:47-57(2002) [PubMed] [Europe PMC] [Abstract]
  6. "TULP3 bridges the IFT-A complex and membrane phosphoinositides to promote trafficking of G protein-coupled receptors into primary cilia."Genes Dev. 24:2180-2193(2010) [PubMed] [Europe PMC] [Abstract]
  7. "TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum." Nat. Genet. 43:189-196(2011) [PubMed] [Europe PMC] [Abstract]
  8. "Mutations in C5ORF42 cause Joubert syndrome in the French Canadian population."Am. J. Hum. Genet. 90:693-700(2012) [PubMed] [Europe PMC] [Abstract]