Thiol groups of normal immunoglobulin G
نویسندگان
چکیده
منابع مشابه
Thiol Groups of Normal Human Immunoglobulin G By BARBARA
Normal human immunoglobulin G (IgG) was treated with radioactive N-ethylmaleimide in the absence of a reducing agent but in the presence of a denaturing solvent. The sites of reaction were determined by isolation of the radioactive peptides from thermolytic digests ofthe heavy and light chains. Six radioactive peptides were purified from the digest of the light chain and ten from that of the he...
متن کاملA Case of Bruton’s Disease with Normal Immunoglobulin G Level
X-linked agamaglobulinemia (XLA) or Bruton’s disease is a genetic disease resulting from a mutation in the Bruton’s tyrosine kinase (Btk) gene. This mutation leads to B cell arrest during differentiation (1). This disease was first described by Ogden Bruton in 1952 (2). Approximately 85% of the affected subjects are male (3). This disorder is inherited as an X-linked recessive trait. Carrier fe...
متن کاملa case of bruton’s disease with normal immunoglobulin g level
x-linked agamaglobulinemia (xla) or bruton’s disease is a genetic disease resulting from a mutation in the bruton’s tyrosine kinase (btk) gene. this mutation leads to b cell arrest during differentiation (1). this disease was first described by ogden bruton in 1952 (2). approximately 85% of the affected subjects are male (3). this disorder is inherited as an x-linked recessive trait. carrier fe...
متن کاملIsoclinic Classification of Some Pairs $(G,G\')$ of $p$-Groups
The equivalence relation isoclinism partitions the class of all pairs of groups into families. In this paper, a complete classification of the set of all pairs $(G,G')$ is established, whenever $G$ is a $p$-group of order at most $p^5$ and $p$ is a prime number greater than 3. Moreover, the classification of pairs $(H,H')$ for extra special $p$-groups $H$ is also given.
متن کاملA case of Bruton's disease with normal immunoglobulin G level.
X-linked agamaglobulinemia (XLA) or Bruton’s disease is a genetic disease resulting from a mutation in the Bruton’s tyrosine kinase (Btk) gene. This mutation leads to B cell arrest during differentiation (1). This disease was first described by Ogden Bruton in 1952 (2). Approximately 85% of the affected subjects are male (3). This disorder is inherited as an X-linked recessive trait. Carrier fe...
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ژورنال
عنوان ژورنال: Biochemical Journal
سال: 1974
ISSN: 0264-6021
DOI: 10.1042/bj1370281