anti-Keratin Basic Antibodies

The protein encoded by is a member of the keratin gene family.

list all antibodies Gene Name GeneID UniProt
Anti-Human  3848 P04264
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Top anti-Keratin Basic Antibodies at antibodies-online.com

Showing 10 out of 118 products:

Catalog No. Reactivity Host Conjugate Application Images Quantity Supplier Delivery Price Details
Human Rabbit CF®405S FACS, IF, IHC, WB   100 μL Log in to see 3 to 4 Days
$157.54
Details
Human Rabbit CF405M FACS, IF, IHC, WB   100 μL Log in to see 3 to 4 Days
$157.54
Details
Human Rabbit CF®640R FACS, IF, IHC, WB   100 μL Log in to see 3 to 4 Days
$157.54
Details
Human Rabbit CF®543 FACS, IF, IHC, WB   100 μL Log in to see 3 to 4 Days
$157.54
Details
Human Rabbit CF®647 FACS, IF, IHC, WB   100 μL Log in to see 3 to 4 Days
$157.54
Details
Human Rabbit CF®555 FACS, IF, IHC, WB   100 μL Log in to see 3 to 4 Days
$157.54
Details
Human Rabbit CF®660R FACS, IF, IHC, WB   100 μL Log in to see 3 to 4 Days
$157.54
Details
Human Rabbit CF®568 FACS, IF, IHC, WB   100 μL Log in to see 3 to 4 Days
$157.54
Details
Human Rabbit CF®770 FACS, IF, IHC, WB   100 μL Log in to see 3 to 4 Days
$157.54
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Human Rabbit CF®680 FACS, IF, IHC, WB   100 μL Log in to see 3 to 4 Days
$157.54
Details

More Antibodies against Keratin Basic Interaction Partners

Human Keratin Basic interaction partners

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

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

  3. Case Report: post-zygotic mosaicism of KRT/1o mutations in epidermolytic Ichthyosis (show LBR Antibodies).

  4. 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.

  5. Report genetic/clinical spectrum of KRT1 mutations in keratinopathic ichthyosis (show LBR Antibodies).

  6. 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

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

  8. Complete structure of an epithelial keratin 1/keratin 10 (show KRT10 Antibodies) dimer has been presented.

  9. These findings indicate that exogenous FABP4 (show FABP4 Antibodies) interacts with plasma membrane proteins, specifically CK1 (show CSNK1A1L Antibodies).

  10. analysis of a heterozygous novel splice junction mutation in the 2B domain of KRT1 in a family with diffuse palmoplantar keratoderma

Keratin Basic Antigen Profile

Protein 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 anti-Keratin Basic Antibodies

  • keratin 1 (KRT1) antibody
  • CK1 antibody
  • EHK antibody
  • EHK1 antibody
  • EPPK antibody
  • K1 antibody
  • KRT1A antibody
  • NEPPK antibody

Protein level used designations for anti-Keratin Basic Antibodies

67 kDa cytokeratin , CK-1 , cytokeratin 1 , cytokeratin-1 , epidermolytic hyperkeratosis 1 , hair alpha protein , keratin, type II cytoskeletal 1 , type-II keratin Kb1

GENE ID SPECIES
3848 Homo sapiens
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