KRT16
Reaktivität: Human
Wirt: Maus
Monoclonal
LL025
unconjugated
Applikationshinweise
KRT16 antibody can be used for detection of KRT16 by ELISA at 1:312500. KRT16 antibody can be used for detection of KRT16 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
Beschränkungen
Nur für Forschungszwecke einsetzbar
Format
Lyophilized
Rekonstitution
Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.
Konzentration
1 mg/mL
Buffer
Antibody is lyophilized in PBS buffer with 2 % sucrose.
Handhabung
As with any antibody avoid repeat freeze-thaw cycles.
Lagerung
4 °C/-20 °C
Informationen zur Lagerung
For short periods of storage (days) store at 4 °C. For longer periods of storage, store KRT16 antibody at -20 °C.
CK16 antikoerper, FNEPPK antikoerper, K16 antikoerper, K1CP antikoerper, KRT16A antikoerper, NEPPK antikoerper, AI324768 antikoerper, Krt1-16 antikoerper, Ka16 antikoerper, KRT16 antikoerper, Krt16 antikoerper, keratin 16 antikoerper, keratin 16, type I S homeolog antikoerper, keratin, type I cytoskeletal 16 antikoerper, KRT16 antikoerper, Krt16 antikoerper, krt16.S antikoerper, LOC101108147 antikoerper, LOC100714013 antikoerper
Hintergrund
KRT16 is a member of the keratin gene family. The keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into cytokeratins and hair keratins. Most of the type I cytokeratins consist of acidic proteins which are arranged in pairs of heterotypic keratin chains and are clustered in a region of chromosome 17q12-q21. This keratin has been coexpressed with keratin 14 in a number of epithelial tissues, including esophagus, tongue, and hair follicles.The protein encoded by this gene is a member of the keratin gene family. The keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into cytokeratins and hair keratins. Most of the type I cytokeratins consist of acidic proteins which are arranged in pairs of heterotypic keratin chains and are clustered in a region of chromosome 17q12-q21. This keratin has been coexpressed with keratin 14 in a number of epithelial tissues, including esophagus, tongue, and hair follicles. Mutations in this gene are associated with type 1 pachyonychia congenita, non-epidermolytic palmoplantar keratoderma and unilateral palmoplantar verrucous nevus. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.