Corneodesmosin (CDSN) Kits ELISA

CDSN encodes a protein found in corneodesmosomes, which localize to human epidermis and other cornified squamous epithelia. De plus, nous expédions Corneodesmosin Anticorps (42) et Corneodesmosin Protéines (10) et beaucoup plus de produits pour cette protéine.

list all ELISA KIts Gène GeneID UniProt
CDSN 1041 Q15517
CDSN 386463 Q7TPC1
CDSN 406198  
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Top Corneodesmosin Kits ELISA sur anticorps-enligne.fr

Showing 10 out of 32 products:

Catalogue No. Reactivité Sensibilité Gamme Images Quantité Livraison Prix Détails
Humain 0.055 ng/mL 0.15 ng/mL - 10 ng/mL 96 Tests 13 to 16 Days
$736.84
Détails
Lapin 0.1 ng/mL 0.5-10 ng/mL 96 Tests 15 to 18 Days
$707.14
Détails
Souris 19.53 pg/mL n/a   96 Tests 15 to 18 Days
$910.56
Détails
Rat 0.1 ng/mL 0.5-10 ng/mL   96 Tests 15 to 18 Days
$707.14
Détails
Cobaye 0.1 ng/mL 0.5-10 ng/mL   96 Tests 15 to 18 Days
$707.14
Détails
Poulet 0.094 ng/mL 0.156-10 ng/mL   96 Tests 12 to 14 Days
$715.00
Détails
Porc 0.094 ng/mL 0.156-10 ng/mL   96 Tests 12 to 14 Days
$715.00
Détails
Singe 0.1 ng/mL 0.5-10 ng/mL   96 Tests 15 to 18 Days
$707.14
Détails
Chien 0.1 ng/mL 0.5-10 ng/mL   96 Tests 15 to 18 Days
$707.14
Détails
Humain 1.23 pg/mL n/a   96 Tests 11 to 16 Days
$693.00
Détails

Plus Kits ELISA pour Corneodesmosin partenaires d'interaction

Human Corneodesmosin (CDSN) interaction partners

  1. results show, for the first time, the male-only associations of the PSORS1C3 gene with psoriasis risk and of the PSORS1C1/CDSN gene with severity of disease. However, the age dependent associations need to be validated in larger sample sizes as well as in other populations.

  2. We found that a burden of low-frequency coding variants in N4BP2, CDSN, PRTG, and AHRR were associated with increased risk of Nonsyndromic cleft lip with or without cleft palate (NSCL/P) . Low-frequency variants in other genes were associated with decreased risk of NSCL/P. These results demonstrate that low-frequency variants contribute to the genetic etiology of NSCL/P

  3. Investigated potential direct protein-protein interactions between six late cornified envelope (LCE) proteins and two corneodesmosin sequence variants. Partial colocalization of LCE2 and CDSN was observed in normal and psoriasis skin.

  4. we report a patient with PSD caused by a novel homozygous large deletion in the 6p21.3 region encompassing the CDSN gene, which abrogates CDSN expression

  5. Case Report: homozygous deletion of CDSN was considered to be responsible for generalized peeling skin disease.

  6. PSORS1C1/CDSN gene may play a pathogenic role in ankylosing spondylitis

  7. A nonsense mutation (C717G) in cDNA sequence of the CDSN gene was identified in all three patients of the family.

  8. CDSN -619C/T polymorphism may not be associated with susceptibility to psoriasis.

  9. CDSN plays a vital role in the structural and functional integrity of the epidermis and the hair follicle integrity by preventing the rupture of corneodesmosome.

  10. identified mRNA transcripts from three genes CDSN, LOR and KRT9, showing strong over-expression in skin samples relative to samples from forensic body fluids, making them suitable markers for skin identification

  11. Study of consangunity in a large family points to a homozygous nonesense mutation of the gene coding for corneodesmosin.

  12. The distribution of corneodesmosin on the surface of the stratum corneum was mapped at the nanoscale using atomic force microscopy.

  13. Data identifies hypotrichosis simplex of the scalp as a human amyloidosis related to the aggregation of natively unfolded (mut)CDSN polypeptides into amyloid fibrils.

  14. Lack of corneodesmosin causes an epidermal barrier defect supposed to account for the predisposition to atopic diseases.

  15. identified nonsense mutations in the gene CDSN (encoding corneodesmosin) in three families suffering from hypotrichosis simplex of the scalp

  16. non-glycosylated CDSN is able to spontaneously form large homo-oligomers in vitro and that the N-terminal glycine loop domain is necessary for the formation of these macromolecular complexes.

  17. Association analyses show that haplotypes bearing CDSN*971T maps to a RNA stability motif and confers psoriasis susceptibility in a wide range of ethnic groups.

  18. phenotype of Netherton syndrome is a consequence of desmosomal fragility associated with premature proteolysis of corneodesmosin

Mouse (Murine) Corneodesmosin (CDSN) interaction partners

  1. These results underscore the essential roles of CDSN in hair physiology and suggest functional relevance of CDSN gene polymorphisms to psoriasis susceptibility.

Corneodesmosin (CDSN) profil antigène

Antigen Summary

This gene encodes a protein found in corneodesmosomes, which localize to human epidermis and other cornified squamous epithelia. During maturation of the cornified layers, the protein undergoes a series of cleavages, which are thought to be required for desquamation. The gene is located in the major histocompatibility complex (MHC) class I region on chromosome 6.

Gene names and symbols associated with Corneodesmosin (CDSN) Kits ELISA

  • corneodesmosin (CDSN) anticorps
  • corneodesmosin (Cdsn) anticorps
  • AI747712 anticorps
  • D6S586E anticorps
  • HTSS anticorps
  • HTSS1 anticorps
  • PSS anticorps
  • S anticorps

Protein level used designations for Corneodesmosin (CDSN) Kits ELISA

corneodesmosin , differentiated keratinocyte S protein , s protein

GENE ID SPECIES
100529069 Ornithorhynchus anatinus
1041 Homo sapiens
386463 Mus musculus
406198 Rattus norvegicus
100735014 Cavia porcellus
100144482 Sus scrofa
607062 Canis lupus familiaris
522351 Bos taurus
101109128 Ovis aries
714553 Macaca mulatta
462553 Pan troglodytes
100338321 Oryctolagus cuniculus
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