Work with LifeSpan to design a custom immunohistochemistry to address your specific biological question. Outsource the entire localization process without having to
worry about finding and characterizing target specific antibodies, sourcing and validating difficult-to-find tissues, and having the ability to interpret the resulting
immunostaining in relation to complex human pathologies.
TCR Screening Services
Test your therapeutic antibodies in immunohistochemistry against a broad panel of normal frozen human tissue types in order to determine potential unintended binding.
Our non-GLP TCR services are designed on the FDA recommendation outlined in their "Points to Consider in the Manufacture and Testing of Monoclonal Antibody Products for Human Use".
Rabbit Polyclonal to Human KRT2 / CK2 / Cytokeratin 2
Human, Mouse, Rat
IHC, Western blot, Immunoprecipitation, ELISA
Mouse Monoclonal [clone Ks2,342,7,1] (IgG1) to Human KRT2 / CK2 / Cytokeratin 2
Human, Mouse, Rat, Bovine
IHC - Paraffin, IHC - Frozen, Western blot, Immunoprecipitation
Human KRT2 / CK2 / Cytokeratin 2
Human, Mouse, Rat, Bovine (tested or 100% immunogen sequence identity)
IgG1 Monoclonal [Ks2,342,7,1]
IHC - Paraffin (1:50)
IHC - Frozen
Specificity and Use
KRT2 / CK2 / Cytokeratin 2 antibody was raised against basic human keratin K2
Also designated cytokeratin 2e; reactive with epidermalcells in uppermost suprabasal layers; recognizes individual cells within epidermis of tongue and mamille (co-localization with keratin K10); also reactive on hyperkeratosis of diverse viral and genetic origin.
PBS containing 0.09% sodium azide.
Short term 4°C, long term aliquot and store at -20°C, avoid freeze thaw cycles. Store undiluted.
KRT2 / CK2 / Cytokeratin 2 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 expressed largely in the upper spinous layer of epidermal keratinocytes and mutations in this gene have been associated with bullous congenital ichthyosiform erythroderma.