Coiled-Coil Domain Containing 40 (CCDC40) ELISA Kits

CCDC40 encodes a protein that is necessary for motile cilia function. Additionally we are shipping CCDC40 Antibodies (19) and CCDC40 Proteins (3) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
CCDC40 55036 Q4G0X9
CCDC40 207607 Q8BI79
CCDC40 287867  
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Top CCDC40 ELISA Kits at antibodies-online.com

Showing 10 out of 13 products:

Catalog No. Reactivity Sensitivity Range Images Quantity Supplier Delivery Price Details
Human 1.0 pg/mL 50-1000 pg/mL 96 Tests Log in to see 15 to 18 Days
$707.14
Details
Rat 1.0 pg/mL 50-1000 pg/mL   96 Tests Log in to see 15 to 18 Days
$707.14
Details
Mouse 1.0 pg/mL 50-1000 pg/mL   96 Tests Log in to see 15 to 18 Days
$707.14
Details
Monkey 1.0 pg/mL 50-1000 pg/mL   96 Tests Log in to see 15 to 18 Days
$707.14
Details
Rabbit 1.0 pg/mL 50-1000 pg/mL   96 Tests Log in to see 15 to 18 Days
$707.14
Details
Guinea Pig 1.0 pg/mL 50-1000 pg/mL   96 Tests Log in to see 15 to 18 Days
$707.14
Details
Dog 1.0 pg/mL 50-1000 pg/mL   96 Tests Log in to see 15 to 18 Days
$707.14
Details
Goat
  96 Tests Log in to see 15 to 18 Days
$707.14
Details
Chicken
  96 Tests Log in to see 15 to 18 Days
$707.14
Details
Cow
  96 Tests Log in to see 15 to 18 Days
$707.14
Details

More ELISA Kits for CCDC40 Interaction Partners

Human Coiled-Coil Domain Containing 40 (CCDC40) interaction partners

  1. Results identified a novel mutant alleles in CCDC40 gene, which altered the protein sequence and resulted in the ultrastructural defects in the microtubule structure of cilia suggesting that CCDC40 mutation may be a cause for ciliary dyskinesia.

  2. Lung disease was worse in those with IDA (show IDUA ELISA Kits)/CA/MTD (show MT1E ELISA Kits) ultrastructural defects, most of whom had biallelic mutations in ccdc40.

  3. This study shows that CCDC39 (show CCDC39 ELISA Kits) and CCDC40 mutations are the major cause of Primary ciliary dyskinesia in patients with the previously termed "radial spoke defect".

  4. Aiming to delineate the CCDC39/CCDC40 mutation spectrum and associated phenotypes, a large cohort of patients with IDA defects were screened. Biallelic CCDC39 or CCDC40 mutations were identified in 30/34 unrelated families with IDA defects.

  5. CCDC40 mutations in humans result in a variant of primary ciliary dyskinesia characterized by misplacement of the central pair of microtubules and defective assembly of inner dynein arms and dynein regulatory complexes.

Mouse (Murine) Coiled-Coil Domain Containing 40 (CCDC40) interaction partners

CCDC40 Antigen Profile

Antigen Summary

This gene encodes a protein that is necessary for motile cilia function. It functions in correct left-right axis formation by regulating the assembly of the inner dynein arm and the dynein regulatory complexes, which control ciliary beat. Mutations in this gene cause ciliary dyskinesia type 15, a disorder due to defects in cilia motility. Alternative splicing results in multiple transcript variants.

Gene names and symbols associated with CCDC40

  • coiled-coil domain containing 40 (CCDC40) antibody
  • coiled-coil domain containing 40 (Ccdc40) antibody
  • coiled-coil domain containing 40 (ccdc40) antibody
  • B930008I02Rik antibody
  • CILD15 antibody
  • im:7149866 antibody
  • lok antibody
  • si:dkey-237i9.5 antibody
  • wu:fb11d02 antibody

Protein level used designations for CCDC40

coiled-coil domain-containing protein 40 , protein links , protein locke

GENE ID SPECIES
55036 Homo sapiens
207607 Mus musculus
483351 Canis lupus familiaris
100514181 Sus scrofa
529788 Bos taurus
287867 Rattus norvegicus
568590 Danio rerio
100733015 Cavia porcellus
101110430 Ovis aries
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