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Keratin 84 Anticuerpo(N-15): sc-168321

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(Basado en el análisis de datos)
  • Keratin 84 Antibody (N-15) is a goat polyclonal IgG provided at 200 µg/ml
  • epitope mapping near the N-terminus of Keratin 84 of human origin
  • recommended for detection of Keratin 84 of human and rat origin by WB, IF and ELISA; non cross-reactive with other Keratin family members; also reactive with additional species, including bovine
  • blocking peptide, sc-168321 P
 

Ver tambiénKeratin AntibodiesincluyebdoKeratin, Keratin 24, Keratin 26, Keratin 39, Keratin 42, Keratin 6B, Keratin 71, Keratin 75, Keratin 83, Keratin 85, Keratin 2, Keratin 25, Keratin 27, Keratin 28, Keratin 31, Keratin 32, Keratin 33B, Keratin 34, Keratin 35, Keratin 36, Keratin 37, Keratin 38, Keratin 40, Keratin 72, Keratin 73, Keratin 74, Keratin 76, Keratin 77, Keratin 78, Keratin 79, Keratin 80, Keratin 81, Keratin 82, Keratin 84yKeratin 86.

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 Información sobre pedidos
Nombre del productoNúmero de catálogoUnidadPrecioCantidadAñadir 
Keratin 84 Antibody (N-15) sc-168321 200 µg/ml $279
Keratin 84 (N-15) P sc-168321 P
(peptide)
 100 µg/0.5 ml $61
 
Especies Nombre del Gen Gene ID Ubicación en el cromosoma Numero de Acceso de Isoforma (ARNm) Número de Acceso de la Proteína Número OMIM™:
Humano KRT84 3890 12q13.12 NM_033045 Q9NSB2
 602766
 

The Keratin multigene family is made of “soft” epithelial cytokeratins and “hard” hair Keratins. While the epithelial cytokeratins are involved in the layering and formation of epithelia, the hair Keratins are responsible for creating nails and hair. There are two types of Keratins: the acidic class I Keratin proteins and the basic/neutral class II Keratin proteins. Keratin 84, also known as KRT84, HB4 or KRTHB4, is a 600 amino acid protein that is expressed in hair follicles. Keratin 84 is a basic/neutral type II Keratin protein which heterodimerizes with type I Keratins to create hair and nails. The gene encoding Keratin 84 maps to human chromosome 12 which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis and Kniest dysplasia.