Browse our anti-TTC21B (TTC21B) Antibodies

Full name:
anti-Tetratricopeptide Repeat Domain 21B Antibodies (TTC21B)
On are 18 Tetratricopeptide Repeat Domain 21B (TTC21B) Antibodies from 3 different suppliers available. Additionally we are shipping and many more products for this protein. A total of 20 TTC21B products are currently listed.
2410066K11Rik, aln, ATD4, IFT139, JBTS11, mKIAA1992, NPHP12, RGD1565122, Thm1, ttc21b
list all antibodies Gene Name GeneID UniProt
TTC21B 79809 Q7Z4L5
TTC21B 73668 Q0HA38
TTC21B 295654  

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anti-Human TTC21B Antibodies:

anti-Mouse (Murine) TTC21B Antibodies:

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Top referenced anti-TTC21B Antibodies

  1. Human Polyclonal TTC21B Primary Antibody for IHC, IHC (p) - ABIN4363272 : Xu, Cao, Huang, Feng, Zhang, Zhu, Yan: Characterization of tetratricopeptide repeat-containing proteins critical for cilia formation and function. in PLoS ONE 2015 (PubMed)

More Antibodies against TTC21B Interaction Partners

Human Tetratricopeptide Repeat Domain 21B (TTC21B) interaction partners

  1. TTC21B mutation is associated with glomerular and cystic kidney diseases.

  2. Exome sequencing and further CRB2 (show CRB2 Antibodies) analysis revealed that both siblings are compound heterozygotes for CRB2 (show CRB2 Antibodies) mutations p.N800K and p.Gly1036Alafs*43, and heterozygous for a deleterious splice variant in the ciliopathy gene TTCB21

  3. We demonstrated that the TTC21B gene product IFT139, an intraflagellar transport-A component, mainly localizes at the base of the primary cilium in developing podocytes from human fetal tissue and in undifferentiated cultured podocytes.

  4. TTC21B contributes pathogenic alleles to approximately 5% of ciliopathy cases. Our data illustrate how genetic lesions can be both causally associated with diverse ciliopathies and interact in trans with other disease-causing genes

Mouse (Murine) Tetratricopeptide Repeat Domain 21B (TTC21B) interaction partners

  1. genetically ablated Kif3a (show KIF3A Antibodies), Ift88 (show IFT88 Antibodies), and Ttc21b in a series of specific spatiotemporal domains. The resulting phenotypes allow us to draw several conclusions. First, we conclude that the Ttc21b cortical phenotype is not due to the activity of Ttc21b within the brain itself

  2. loss of Thm1 causes cystic kidney disease, with persistent proliferation of renal cells, elevated cAMP levels, and enhanced expression of Hedgehog (show SHH Antibodies) signaling genes

  3. Data characterize the forebrain phenotype caused by loss of Ttc21b, a gene we identified in an ENU mutagenesis screen as a novel ciliary gene required for retrograde intraflagellar transport.

TTC21B Antigen Profile

Antigen Summary

This gene encodes a member of TTC21 family, containing several tetratricopeptide repeat (TPR) domains. This protein is localized to the cilium axoneme, and may play a role in retrograde intraflagellar transport in cilia. Mutations in this gene are associated with various ciliopathies, nephronophthisis 12, and asphyxiating thoracic dystrophy 4.

Alternative names and synonyms associated with TTC21B

  • tetratricopeptide repeat domain 21B (TTC21B) antibody
  • tetratricopeptide repeat domain 21A (ttc21a) antibody
  • tetratricopeptide repeat domain 21B (Ttc21b) antibody
  • 2410066K11Rik antibody
  • aln antibody
  • ATD4 antibody
  • IFT139 antibody
  • JBTS11 antibody
  • mKIAA1992 antibody
  • NPHP12 antibody
  • RGD1565122 antibody
  • Thm1 antibody
  • ttc21b antibody

Protein level used designations for TTC21B

TPR repeat protein 21B , tetratricopeptide repeat protein 21B , putative protein product of Nbla10696 , line 158 , tetratricopeptide repeat-containing hedgehog modulator 1

100052001 Equus caballus
432176 Xenopus laevis
79809 Homo sapiens
73668 Mus musculus
608674 Canis lupus familiaris
100516342 Sus scrofa
527412 Bos taurus
295654 Rattus norvegicus
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