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Keratin 3 (KRT3) ELISA Kits

The protein encoded by KRT3 is a member of the keratin gene family. Additionally we are shipping Keratin 3 Antibodies (23) and Keratin 3 Proteins (4) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
Anti-Mouse KRT3 KRT3 12709 Q04447
Anti-Human KRT3 KRT3 3850 P12035
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More ELISA Kits for Keratin 3 Interaction Partners

Mouse (Murine) Keratin 3 (KRT3) interaction partners

  1. Loss of normal CKB (show CHKB ELISA Kits) structure and function contributes to the mechanisms by which isoaspartate accumulation leads to central nervous system dysfunction in the PIMT (show PCMT1 ELISA Kits)-Knockout mouse.

  2. CKB (show CHKB ELISA Kits) plays a key role in myotube formation by limiting myoblast fusion during myogenesis.

  3. BCK (show CKB ELISA Kits) phosphorylation at Ser6 did not affect its enzymatic activity, but led to the appearance of the phosphorylated enzyme at the endoplasmic reticulum (ER)

  4. Hypothalamic plasticity of neuropeptide Y (show NPY ELISA Kits) is lacking in brain-type creatine kinase double knockout mice with defective thermoregulation

  5. negative regulation of CKB (show CHKB ELISA Kits) by mHTT is a key event in the pathogenesis of HD and contributes to the neuronal dysfunction associated with HD.

  6. reduced expression of brain creatine kinase (show CKB ELISA Kits) in the cochlea of Huntington disease (show HTT ELISA Kits) mice is associated with hearing impairment

  7. In rat cerebrum and cerebellum, as in rat heart, at all ages the several cCK (show CCK ELISA Kits) isoenzymes do participate in a gender-specific manner, in favor of females, in diverse functions of the different cell compartments of glial and neuronal cells.

  8. cytoskeletal dynamics during cell motility is coupled to on-site availability of ATP generated by CKB (show CHKB ELISA Kits)

Human Keratin 3 (KRT3) interaction partners

  1. Exon sequencing of KRT3 and KRT12 (show KRT12 ELISA Kits) in six affected and eight unaffected individuals did not detect any mutations or nucleotide sequence variants in Meesmann epithelial corneal dystrophy.

  2. A novel missense mutation (R503P) in KRT3 leads to MCD in 2 unrelated Taiwanese families.

  3. Location of the E498V mutation emphasizes the functional relevance of the highly conserved boundary motifs at the COOH-terminus of the alpha-helical rod domain in keratin 3 (K3).

Keratin 3 (KRT3) 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 corneal epithelium with family member KRT12 and mutations in these genes have been associated with Meesmann's Corneal Dystrophy. The type II cytokeratins are clustered in a region of chromosome 12q12-q13.

Gene names and symbols associated with Keratin 3 (KRT3) ELISA Kits

  • keratin 3 (KRT3) antibody
  • creatine kinase, brain (Ckb) antibody
  • B-CK antibody
  • Bck antibody
  • CK-3 antibody
  • CK3 antibody
  • Ckbb antibody
  • K3 antibody

Protein level used designations for Keratin 3 (KRT3) ELISA Kits

keratin 3 , cytokeratin Ib (human cytokeratin 3) , creatine kinase B chain , creatine kinase B-type , 65 kDa cytokeratin , CK-3 , cytokeratin 3 , cytokeratin-3 , keratin, type II cytoskeletal 3 , type-II keratin Kb3 , K3 keratin , Type-II keratin Kb3 , keratin K3

281267 Bos taurus
12709 Mus musculus
3850 Homo sapiens
100353668 Oryctolagus cuniculus
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