𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A new V gene expressed in lambda-2 light chains of the mouse

✍ Scribed by Renate Dildrop; Angela Gause; Werner Müller; Klaus Rajewsky


Publisher
John Wiley and Sons
Year
1987
Tongue
English
Weight
492 KB
Volume
17
Category
Article
ISSN
0014-2980

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


The level of λ1 light chain expression i
✍ Daniele Primi; Matthieu Levi-Strauss; Pierre-André Cazenave 📂 Article 📅 1986 🏛 John Wiley and Sons 🌐 English ⚖ 811 KB

## Immunochimie Analytique' and Unit6 d'ImmunogCnCtique', Institut Pasteur, Paris The predominance of x over h light chain expression in mice can either reflect the probability of rearrangement of the relevant locus or be the result of antigen-driven clonal expansion. To discriminate between these

Regulation of collagen gene expression i
✍ Tatjana Barisic-Dujmovic; Ivana Boban; Stephen H. Clark 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 409 KB

## Abstract The tight skin 2 (Tsk2) mutation is an ENU induced dominant mutation localized on mouse chromosome 1. While the molecular defect is unknown, Tsk2/+ mice display cutaneous thickening associated with excessive matrix production and are used as a model of scleroderma. The purpose of this s

Expression of a mouse Ig V gene in antib
✍ Thereza Imanishi; M. Hurme; Heikki Sarvas; O. Mäkelä 📂 Article 📅 1975 🏛 John Wiley and Sons 🌐 English ⚖ 509 KB

## Abstract In an earlier study we found that some mouse strains, including the C57BL/6, produced irregular IgG anti‐(4‐hydroxy‐3‐nitrophenyl)acetyl (NP) antibodies to protein conjugates of this hapten. This antibody had heteroclitic fine specificity and a characteristic isoelectric focusing patter

The chicken Ig light chain 3′-enhancer i
✍ Thomas M. Conlon; Kerstin B. Meyer 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 307 KB

## Abstract Expression of the rearranged chicken immunoglobulin light chain (IgL) gene is regulated by a V gene promoter, a matrix attachment region (MAR) in the J‐C intron and an enhancer downstream of the Ig constant region. Using knockout analysis, we demonstrate that the 3′‐enhancer is not only