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Almost full conversion of the borate glass to hydroxyapatite was achieved in less than 6 days.
Conversion of the borate glass to hydroxyapatite was investigated by soaking the constructs in a solution of K2HPO4 (0.25 M) at 37 °C and with a pH value of 9.0, and measuring the weight loss of the constructs as a function of time.
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The conversion product of the borate glass was identified by XRD, SEM.
In addition, the conversion of magnesium borate hydroxide to anhydrous magnesium borate is rarely reported [7, 21].
The reaction of NHS PEG with amino-modified single stranded RNA oligonucleotides afforded nearly complete conversion of the oligonucleotide after 3 h at room temperature in a borate buffer as monitored by HPLC.
Seawater is the source of virtually all of the borate in altered oceanic crust.
The cell growth inhibition rate of the borate glass was examined by MTT assay.
Figure 3 shows the composition of the borate layers.
These findings indicate that the borate-dependent degradation machinery of the borate transporter is conserved among plant species.
Interestingly, the authors showed that de novo synthesis of the borate-dependent degradation machinery of the borate transporter BOR1 is required for maintaining the degradation.
Rather than comparing Lb of the borate anion with L a of the cations, Becker looked only at the bonding strengths of the cations, using them to infer the bonding strengths of the various kinds of borate anions.
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