摘要:
The present invention first provides monoclonal antibodies recognizing membrane phospholipase A₂, namely, monoclonal antibodies PL-49, PL-71, PL-76, and PL-78, hybridomas producing them, methods for producing them, and immunoassays of membrane phospholipase A₂ using them. The immunoassay of PLA₂M is useful for the diagnosis of articular rheumatism, cancers, and a wide variety of inflammatory states.
摘要:
This invention provides an immunoassay of elastase-1, which comprises subjecting (a) labelled elastase-1 treated with Boc-TACK and (b) elastase-1 to be measured to competitive reaction with anit-elastase-1 antibody, wherein the Boc-TACK denotes (CH₃)₃COCO[NHCH(CH₃)CO]₃CH₂Cl.
摘要:
The present invention first provides monoclonal antibodies recognizing membrane phospholipase A₂, namely, monoclonal antibodies PL-49, PL-71, PL-76, and PL-78, hybridomas producing them, methods for producing them, and immunoassays of membrane phospholipase A₂ using them. The immunoassay of PLA₂M is useful for the diagnosis of articular rheumatism, cancers, and a wide variety of inflammatory states.
摘要:
A monoclonal antibody recognizing a reg protein and a hybridoma producing the monoclonal antibody are provided. Also, methods for the assay of a reg protein using the monoclonal antibody are provided.
摘要:
A new reg protein is provided. The reg protein has an amino acid sequence beginning with the glutamine residue at the 20th position from the amino terminus and terminating with the asparagine residue at the 165th position in Figure 1, or an amino acid sequence containing an additional methionine residue at the amino terminus of said amino acid sequence extending from the glutamine residue to the asparagine residue.
摘要:
A novel method for producing glucagon is provided. The method comprises the steps of, preparing a fusion protein shown by the following formula: X-Glu-Glucagon (I) wherein X is a leader sequence of 70-170 amino acids, Glu is a glutamic acid residue, and Glucagon represents the amino acid sequence of glucagon, and treating the fusion protein with an enzyme that specifically hydrolyzes the peptide bonds at the carboxyl termini of the glutamic acid residues, resulting in cleavage of the fusion protein.
摘要:
A novel protease derived from Bacillus licheniformis is provided. The protease cleaves the peptide bonds at the carboxyl termini of glutamic acid residues in polypeptides. The protease contains an amino acid sequence from serine in the +1 position to glutamine in the +222 position of SEQ ID NO: 1.
摘要翻译:提供了一种来源于地衣芽孢杆菌的新型蛋白酶。 蛋白酶切割多肽中谷氨酸残基羧基末端的肽键。 蛋白酶含有从+1位的丝氨酸到SEQ ID NO:1的+222位的谷氨酰胺的氨基酸序列。
摘要:
A novel protease derived from Bacillus licheniformis is provided. The protease cleaves the peptide bonds at the carboxyl termini of glutamic acid residues in polypeptides. The protease contains an amino acid sequence from serine in the +1 position to glutamine in the +222 position of SEQ ID NO: 1.
摘要翻译:提供了一种衍生自地衣芽孢杆菌的新型蛋白酶。 蛋白酶切割多肽中谷氨酸残基羧基末端的肽键。 蛋白酶含有从+1位的丝氨酸到SEQ ID NO:1的+222位的谷氨酰胺的氨基酸序列。