Dynein, Axonemal, Heavy Chain 11 (DNAH11) ELISA Kits

DNAH11 encodes a ciliary outer dynein arm protein and is a member of the dynein heavy chain family. Additionally we are shipping DNAH11 Antibodies (20) and DNAH11 Proteins (2) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
DNAH11 8701 Q96DT5
Anti-Mouse DNAH11 DNAH11 13411  
Anti-Rat DNAH11 DNAH11 117253  
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Top DNAH11 ELISA Kits at antibodies-online.com

Showing 2 out of 5 products:

Catalog No. Reactivity Sensitivity Range Images Quantity Delivery Price Details
Human 0.127 ng/mL 0.31 ng/mL - 20 ng/mL 96 Tests 13 to 16 Days
$736.84
Details
Human < 0.127 ng/mL 0.312 ng/mL - 20 ng/mL   96 Tests 11 to 18 Days
$902.56
Details

More ELISA Kits for DNAH11 Interaction Partners

Human Dynein, Axonemal, Heavy Chain 11 (DNAH11) interaction partners

  1. study demonstrated that the polymorphisms rs2494938 at 6p21.1 and rs2285947 at 7p15.3 may serve as independent prognostic biomarkers for ESCC, implying the potential biological role of their related genes (LRFN2 and DNAH11) in the process of ESCC development

  2. DNAH11 mutations result in a characteristic abnormality of the ciliary ultrastructure detectable by electron tomography, but not traditional transmission electron microscopy

  3. Dnah11(avc)(4) did not disrupt SHF Hh signaling and caused Atrioventricular septal defects (AVSDs) only concurrently with heterotaxy, a left/right axis abnormality. In contrast, Mks1(avc)(6) disrupted SHF Hh signaling and caused AVSDs without heterotaxy.We speculate that cilia gene mutations contribute to both syndromic and non-syndromic AVSDs in humans

  4. DNAH11 mutations result in a subtle outer dynein arm defect in only the proximal region of respiratory cilia.

  5. In an epithelial cell line engineered to contain the DNAH11 target site, TALENs cleaved over 80% of the mutated DNAH11 sequence and replaced the mutated sequence with wild-type sequence in about 50% of cells. This study demonstrates that gene editing can rescue ciliary beating ex vivo, opening up new avenues for treating Primary ciliary dyskinesia.

  6. Mutations in DNAH11 are a common cause of PCD in patients without ciliary ultrastructural defects; thus, genetic analysis can be used to ascertain the diagnosis of PCD in this challenging group of patients.

  7. mutations: splice site in acceptor splice site of exon 5 and nonsense mutation located in exon 23 for DNAH11 in primary ciliary dyskinesia

  8. mutations in the DNAH11 gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesia

  9. Dynein plays an unexpected role in the regulation of mitochondrial morphology in living cells, by controlling the recruitment of Drp1 to these organelles.

  10. a specific requirement for p150(Glued)/dynein/functional microtubules in activation of MKK3/6 and p38 MAPKs in vivo.

  11. These findings support the view that DNAH11 mutations indeed cause Primary ciliary dyskinesia and Kartagener syndrome, and that the reported DNAH11 nonsense mutations are associated with a normal axonemal ultrastructure.

  12. Two "major" genes, DNAI1 and DNAH5, underlie PCD in nearly half of the patients with ODA defects

Mouse (Murine) Dynein, Axonemal, Heavy Chain 11 (DNAH11) interaction partners

  1. Dnah11(avc)(4) did not disrupt SHF Hh signaling and caused Atrioventricular septal defects (AVSDs) only concurrently with heterotaxy, a left/right axis abnormality. In contrast, Mks1(avc)(6) disrupted SHF Hh signaling and caused AVSDs without heterotaxy.We speculate that cilia gene mutations contribute to both syndromic and non-syndromic AVSDs in humans

  2. These data unveil a previously unrecognized role for the dynein-dynactin motor complex in osteoclast formation and function.

  3. iv functions to establish asymmetric expression of nodal in a gene-dosage-sensitive manner

  4. work supports the claim that LRD functions in a mechanism for selective chromatid segregation

DNAH11 Antigen Profile

Antigen Summary

This gene encodes a ciliary outer dynein arm protein and is a member of the dynein heavy chain family. It is a microtubule-dependent motor ATPase and has been reported to be involved in the movement of respiratory cilia. Mutations in this gene have been implicated in causing Kartagener Syndrome (a combination of situs inversus totalis and Primary Ciliary Dyskinesia (PCD), also called Immotile Cilia Syndrome 1 (ICS1)) and male sterility.

Gene names and symbols associated with DNAH11

  • dynein axonemal heavy chain 11 (DNAH11) antibody
  • dynein, axonemal, heavy chain 11 (Dnah11) antibody
  • dynein heavy chain 11, axonemal (LOC497208) antibody
  • dynein, axonemal, heavy chain 11 (DNAH11) antibody
  • dynein heavy chain 11, axonemal (LOC100497531) antibody
  • dynein axonemal heavy chain 11 (dnah11) antibody
  • hypothetical protein LOC472305 (DNAH11) antibody
  • dynein axonemal heavy chain 11 L homeolog (dnah11.L) antibody
  • dynein axonemal heavy chain 11 (Dnah11) antibody
  • b2b598Clo antibody
  • b2b1203Clo antibody
  • b2b1279Clo antibody
  • b2b1289Clo antibody
  • b2b1727Clo antibody
  • Bv1 antibody
  • CILD7 antibody
  • DNAHBL antibody
  • Dnahc11 antibody
  • DNHBL antibody
  • DPL11 antibody
  • iv antibody
  • lrd antibody

Protein level used designations for DNAH11

axonemal beta dynein heavy chain 11 , axonemal dynein heavy chain 11 , ciliary dynein heavy chain 11 , dynein heavy chain 11, axonemal , dynein, axonemal, heavy polypeptide 11 , dynein, ciliary, heavy chain 11 , dynein, axon, heavy chain 11 , situs inversus viscerum , dynein, axonemal, heavy chain 11 , dynein heavy chain Bv1 , dynein heavy chain 11, axonemal-like , hypothetical protein LOC472305

GENE ID SPECIES
8701 Homo sapiens
13411 Mus musculus
117253 Rattus norvegicus
482346 Canis lupus familiaris
497208 Bos taurus
100067501 Equus caballus
100497531 Xenopus (Silurana) tropicalis
100566880 Anolis carolinensis
100584743 Nomascus leucogenys
472305 Pan troglodytes
100462917 Xenopus laevis
100518444 Sus scrofa
100733692 Cavia porcellus
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