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Primary Antibodies<br />

Involucrin<br />

Clone SY5<br />

1 mL, 0.1 mL lyophilized NCL-INV F P (Enzyme)<br />

Involucrin is a precursor (120 kD) of the epidermal cornified envelope which<br />

becomes cross-linked during envelope assembly. Involucrin is expressed in<br />

a range of stratified squamous epithelia, including the cornea which lacks a<br />

distinct cornified layer and is expressed when differentiation is terminated.<br />

In normal dermis, involucrin is expressed in the upper cornified layer.<br />

However, in pathological conditions, involucrin expression is altered eg in<br />

psoriasis and other benign epidermal hyperplasias, where involucrin<br />

expression is found closer to the basal layer. Expression of involucrin is<br />

abnormal in squamous cell carcinomas and premalignant lesions.<br />

Product Specific Information<br />

When using NCL-INV, enzyme pretreatment may enhance staining in some<br />

cases.<br />

Kappa Light Chain<br />

Clone CH15 New!<br />

1 mL, 0.1 mL liquid NCL-L-KAP-581 P (HIER)<br />

Clone kp-53<br />

1 mL lyophilized NCL-KAP FPW<br />

Clone L1C1<br />

1 mL, 0.1 mL lyophilized NCL-KAP-L1C1 F P (Enzyme)<br />

Clone L1C1 is the main choice of end users for use on paraffin sections.<br />

Immunoglobulins are polypeptides and comprise five major classes;<br />

immunoglobulin G (IgG), IgA, IgM, IgD and IgE. Each immunoglobulin<br />

consists of two identical heavy (H) chains and two identical light (L) chains.<br />

These are also subdivided into sub classes eg IgG1. There are two classes<br />

of light chain; kappa and lambda. The ratio of kappa chains and light chains<br />

varies between Ig classes and sub classes, but is also species specific. In<br />

humans, approximately 60 percent of light chains are kappa. However, in<br />

any particular immunoglobulin molecule the light chain will be either kappa<br />

or lambda. B cells contain either kappa or lambda mRNA.<br />

Tonsil: immunohistochemical staining for Kappa Light Chain using NCL-L-KAP-581. Note<br />

cytoplasmic staining of plasma cells. Paraffin section.<br />

/ 126<br />

For detailed information on all products please visit our website:<br />

www.leica-microsystems.com<br />

Reference Range<br />

Ki67 Antigen<br />

Clone MM1<br />

1 mL, 0.1 mL lyophilized NCL-Ki67-MM1 F P (HIER)<br />

1 mL liquid NCL-L-Ki67-MM1 F P (HIER)<br />

7 mL ready-to-use RTU-Ki67-MM1 F P (HIER)<br />

7 mL Bond ready-to-use PA0118 P (HIER)<br />

Clone K2 New!<br />

7 mL Bond ready-to-use PA0230 P (HIER)<br />

Polyclonal<br />

0.2 mL lyophilized NCL-Ki67p F P (HIER)<br />

The Ki-67 antigen is a human nuclear protein, which is expressed in all<br />

active parts of the cell cycle (G1, S, G2 and mitosis), but absent in resting<br />

cells (G0). In contrast to many other cell cycle-associated proteins, the Ki67<br />

antigen is consistently absent in quiescent cells and is not detectable during<br />

DNA repair processes. Thus, the presence of Ki67 antigen is strictly<br />

associated with the cell cycle and confined to the nucleus, suggesting an<br />

important role of this structure in the maintenance and/or regulation of the<br />

cell division cycle.<br />

Refer to page 32 for the Bond ready-to-use format.<br />

Kip2 (p57 Protein)<br />

Clone 25B2<br />

1 mL, 0.1 mL lyophilized NCL-p57 P (HIER)<br />

Cyclin dependent kinases are positive regulators of cell proliferation. p57<br />

protein acts as a tumor suppressor to counter this. It is closely-related to<br />

other CDKIs such as p21 protein (CIP1) and p27 protein (Kip1) as they share a<br />

common structural N-terminal domain for binding to CDK/cyclin complexes<br />

and inhibiting their kinase activity. Human p57 protein is found on<br />

chromosome 11p15.5, a region which is reported to be a common site for<br />

loss of heterozygosity in certain sarcomas, Wilms’ tumors and tumors<br />

associated with the Beckwith-Wiedemann syndrome. There is increasing<br />

interest in p57 as a marker in Gestational disease. Gestational trophoblastic<br />

disease refers to a spectrum of proliferative disorders of the placental<br />

trophoblast, with a wide range of histologic appearances and clinical<br />

behaviors. Recent developments in changes in the criteria for histologic<br />

diagnosis of these lesions due to earlier clinical diagnosis have been<br />

reviewed Hui P et al., Advantages in Anatomical Pathology. 12(3): 116-125<br />

(2005) and the ability to make more accurate diagnoses due to the<br />

introduction of newer antibodies such as p57 is discussed.<br />

Products in this catalog are subject to regulatory approval.<br />

This catalog is not for use in the USA.<br />

Reference Range

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