Cytokeratin 1 (KRT1) ELISA Kits

The protein encoded by KRT1 is a member of the keratin gene family. Additionally we are shipping KRT1 Antibodies (511) and KRT1 Proteins (11) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
KRT1 3848 P04264
KRT1 16678 P04104
KRT1 300250 Q6IMF3
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Top KRT1 ELISA Kits at

Showing 10 out of 46 products:

Catalog No. Reactivity Sensitivity Range Images Quantity Supplier Delivery Price Details
Human 0.039 ng/mL 0.156-10 ng/mL Typical standard curve 96 Tests Log in to see 15 to 18 Days
Rat 0.056 ng/mL 0.15 ng/mL - 10 ng/mL 96 Tests Log in to see 13 to 16 Days
Chicken 0.938 ng/mL 1.56 ng/mL - 100 ng/mL   96 Tests Log in to see 11 to 18 Days
Monkey 37.5 pg/mL 62.5 pg/mL - 4000 pg/mL   96 Tests Log in to see 11 to 18 Days
Pig 9.375 pg/mL 15.625 pg/mL - 1000 pg/mL   96 Tests Log in to see 11 to 18 Days
Rabbit 0.375 pg/mL 0.625 pg/mL - 40 pg/mL   96 Tests Log in to see 11 to 18 Days
Guinea Pig 0.094 ng/mL 0.156 ng/mL - 10 ng/mL   96 Tests Log in to see 11 to 18 Days
Sheep 0.469 ng/mL 0.781 ng/mL - 50 ng/mL   96 Tests Log in to see 11 to 18 Days
Human < 0.059 ng/mL 0.156 ng/mL - 10 ng/mL   96 Tests Log in to see 11 to 18 Days
Rat < 0.056 ng/mL 0.156 ng/mL - 10 ng/mL   96 Tests Log in to see 11 to 18 Days

More ELISA Kits for KRT1 Interaction Partners

Human Cytokeratin 1 (KRT1) interaction partners

  1. The authors report a large Italian family affected Palmoplantar Keratoderma and Charcot Marie Tooth disease. Two different mutated genes, KRT1 and MPZ (show MPZ ELISA Kits) were responsible for the two main clinical signs. Exome analysis detected two missense mutations, one in KRT1 and one in MPZ (show MPZ ELISA Kits).

  2. Results show that missense mutations exert dominant negative effects on the keratins K1/K10 (show KRT10 ELISA Kits) protein structure by altering inter-chain interactions.

  3. KRT1 and the specific polymorphism of KRT1 in this Chinese Han population are associated with autoimmune diseases SLE and SSc (show CYP11A1 ELISA Kits)

  4. Case Report: post-zygotic mosaicism of KRT/1o mutations in epidermolytic Ichthyosis.

  5. KRT1 played an important role of maintaining epithelial barrier and its down-regulation in intestinal tissue was correlated with the progression of inflammatory bowel disease.

  6. Report genetic/clinical spectrum of KRT1 mutations in keratinopathic ichthyosis.

  7. demonstrated the presence of a genetic cutaneous mosaicism. Both patients carry the KRT1 pI479T substitution, but in the palmoplantar areas of one of them, only the mutated allele is expressed (hemizygous). This leads to highlight a new type of cutaneous mosaic, the palmoplantar mosaicism

  8. In our study, the missense mutation in the proband and his mother with epidermolytic ichthyosis was a single amino acid difference in codon 478, which causes more serious skin manifestations

  9. Complete structure of an epithelial keratin 1/keratin 10 (show KRT10 ELISA Kits) dimer has been presented.

  10. These findings indicate that exogenous FABP4 (show FABP4 ELISA Kits) interacts with plasma membrane proteins, specifically CK1.

Mouse (Murine) Cytokeratin 1 (KRT1) interaction partners

  1. SCF (show KITLG ELISA Kits) improves diabetic wound healing in part by increasing the recruitment of a unique stem cell population present in the skin.

  2. Absence of Krt1 caused a prenatal increase in interleukin-18 (IL-18 (show IL18 ELISA Kits)) and the S100A8 (show S100A8 ELISA Kits) and S100A9 (show S100A9 ELISA Kits) proteins, accompanied by a barrier defect and perinatal lethality.

  3. The Krt1(-/-);Krt10(-/-) mice showed premature loss of nuclei during epidermal differentiation and lower levels of emerin, lamin A/C and Sun1, revealing a previously unknown function for IFs in maintaining nuclear integrity in the upper epidermis.

KRT1 Antigen Profile

Antigen Summary

The protein encoded by this gene is a member of the keratin gene family. The type II cytokeratins consist of basic or neutral proteins which are arranged in pairs of heterotypic keratin chains coexpressed during differentiation of simple and stratified epithelial tissues. This type II cytokeratin is specifically expressed in the spinous and granular layers of the epidermis with family member KRT10 and mutations in these genes have been associated with bullous congenital ichthyosiform erythroderma. The type II cytokeratins are clustered in a region of chromosome 12q12-q13.

Gene names and symbols associated with Cytokeratin 1 (KRT1) ELISA Kits

  • keratin 1 (KRT1) antibody
  • keratin 1 (Krt1) antibody
  • CK-1 antibody
  • CK1 antibody
  • EHK antibody
  • EHK1 antibody
  • EPPK antibody
  • K1 antibody
  • Kb1 antibody
  • KER1 antibody
  • Keratin-1 antibody
  • Krt-2.1 antibody
  • KRT1 antibody
  • KRT1A antibody
  • Krt2-1 antibody
  • Krt86 antibody
  • NEPPK antibody

Protein level used designations for Cytokeratin 1 (KRT1) ELISA Kits

67 kDa cytokeratin , CK-1 , cytokeratin 1 , cytokeratin-1 , epidermolytic hyperkeratosis 1 , hair alpha protein , keratin, type II cytoskeletal 1 , type-II keratin Kb1 , K1 , keratin 86 , keratin complex 2, basic, gene 1 , keratin-1 , keratin 1 , cytokeratin VI (human cytokeratin 10) , cytokeratin Ia (human cytokeratin 1, epidermolytic hyperkeratosis) , type II keratin Kb1 , epithelial keratin 1 , epithelial keratin-1 , keratin 1 (epidermolytic hyperkeratosis) , Cytokeratin-1 , Keratin, type II cytoskeletal 1

3848 Homo sapiens
16678 Mus musculus
281266 Bos taurus
300250 Rattus norvegicus
444857 Canis lupus familiaris
100049664 Sus scrofa
738375 Pan troglodytes
100353415 Oryctolagus cuniculus
Selected quality suppliers for KRT1 (KRT1) ELISA Kits
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