Abstract: PROBLEM: According to the present invention, a patient who experiences severe bleeding is detected based on a value obtained by a common coagulation test. SOLUTION: The present invention is an analysis method for analyzing the bleeding tendency of a subject, and the problem is resolved by this analysis method which includes obtaining a time-series data set of a coagulation reaction of a blood sample collected from the subject; obtaining, based on the time-series data set, a maximum speed arrival time until a coagulation reaction speed is maximized or a maximum acceleration arrival time until a coagulation reaction acceleration is maximized, and a reference time in the coagulation reaction; obtaining a value based on the maximum speed arrival time or the maximum acceleration arrival time, and the reference time; and outputting the value or information relating to the bleeding tendency based on the value.

Abstract: Promoters capable of efficiently expressing a gene of interest in plants include (1) either a DNA containing SEQ ID No:1 or SEQ ID No:7, or a biological functional equivalent DNA containing SEQ ID No:1 or SEQ ID No:7 that have modifications in their respective nucleotide sequence provided that each retains more than 90% identity to the nucleotide sequence of any region containing at least 250 bp within SEQ ID No:1 or SEQ ID No:7, respectively. Terminators capable of efficiently expressing a gene of interest in plants include either a DNA containing SEQ ID No:2, or a biological functional equivalent DNA containing a SEQ ID No:2 that has a modified nucleotide sequence provided that it retains more than 90% identity to the nucleotide sequence of any region containing at least 250 bp within SEQ ID No:2.

Abstract: The present invention provides a promoter which is characterized in that it has following DNA sequence (a) or (b) and a DNA having the nucleotide sequence shown by SEQ ID:No.1, (a) a DNA sequence having the nucleotide sequence represented by at least nucleotide numbers 112-246 within the nucleotide sequence shown by SEQ ID:No.2, (b) a DNA sequence having the nucleotide sequence represented by at least base numbers 186-282 within the nucleotide sequence shown by SEQ ID:No.3 (hereinafter referred to as the present promoter), a chimera gene having the above promoter, a vector having the above promoter, a transformant characterized in that the promoter, the chimera gene or the vector is introduced into a host cell, a method for expressing gene comprising a step of expressing the desired gene in a host cell under the control of the promoter, use of the promoter for controlling the expression of a desired gene in a host cell, and a method for producing the promoter.