<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Tatik Hernawati</style></author><author><style face="normal" font="default" size="100%">Tita Damayanti Lestari</style></author><author><style face="normal" font="default" size="100%">Suzanita Utama</style></author><author><style face="normal" font="default" size="100%">Rimayanti</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Optimization of Osteopontin Recombinant Protein as a Candidate Supplementation for Semen Preservation</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">DNA clone</style></keyword><keyword><style  face="normal" font="default" size="100%">Osteopontin</style></keyword><keyword><style  face="normal" font="default" size="100%">PCR amplification.</style></keyword><keyword><style  face="normal" font="default" size="100%">Primer</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">668-673</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;The recombinant protein of heterologous proteins in&lt;em&gt; Escherichia coli&lt;/em&gt; strains K12 has various and different systems tested and demands a detailed insight into the multiple factors affecting the encoded protein. One of the crucial factors is the acceptable quality of the DNA copies inserted inside the bacteria. Firstly, the amplification procedure needed to be performed well; thus, designing the primer and selecting the optimum annealing temperature are the focus indicators in this study. This study obtained a reference gene from the NCBI data bank with Reference Sequence: NM_174187.2. Two types of primers (SPP1FSPP1R and OPN1F - OPN1R) with different targeted bands were designed and selected after being reconstructed using the software. Online software such as addgene.org is also used to identify the right restriction site. The annealing temperature distinguished the PCR system used to amplify each primer. The result of this study revealed the best annealing at 65ºC successfully amplified 820 bp of the targeted band. The phenomenon not following the theory of blue-white screening is the empty plasmid control, where not a single colony grows on the media. Competent cells inserted with empty plasmids should still be able to expand on LB-Amp agar media because the presence of these plasmids is capable of providing resistance to antibiotics (in this case, ampicillin). This discrepancy is thought to have been caused by the improper insertion of the empty plasmid so that the plasmid did not enter the competent cell.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">668</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Tatik Hernawati*, Tita Damayanti Lestari, Suzanita Utama, Rimayanti&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Departement of Veterinary Reproduction, Faculty of Veterinary Medicine, Airlangga University, Surabaya, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Amung Logam Saputro</style></author><author><style face="normal" font="default" size="100%">Uliy Ba’sin Syadid</style></author><author><style face="normal" font="default" size="100%">Rimayanti</style></author><author><style face="normal" font="default" size="100%">Suherni Susilowati</style></author><author><style face="normal" font="default" size="100%">Ragil Angga Prastiya</style></author><author><style face="normal" font="default" size="100%">Bodhi Agustono</style></author><author><style face="normal" font="default" size="100%">Fauzan Mumtazi</style></author><author><style face="normal" font="default" size="100%">Marifatunnisa’romadhona</style></author><author><style face="normal" font="default" size="100%">Anastasya</style></author><author><style face="normal" font="default" size="100%">Muhammad Riesta Farhan</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effect of Vitamin C and E Supplementation and Combination of Both in Egg Yolk Tris Diluter on the Quality of Sapera Goat Spermatozoa in the 5 °C Cooling Process</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">5˚C Cooling Process</style></keyword><keyword><style  face="normal" font="default" size="100%">Quality of Spermatozoa</style></keyword><keyword><style  face="normal" font="default" size="100%">Sapera Goat</style></keyword><keyword><style  face="normal" font="default" size="100%">Vitamin C</style></keyword><keyword><style  face="normal" font="default" size="100%">Vitamin E</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">October 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">661-665</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;This study was aimed to determine the effect of vitamin C, E supplementation and both combination in the egg yolk tris diluent on the quality of Sapera goat spermatozoa in 5˚C cooling process. The samples were fresh semen collected from Sapera goat. It was divided into four different treatment groups. The control treatment or P0 contained semen sample + egg yolk tris diluent, P1 contained semen sample + egg yolk tris diluent + vitamin C 0,9 mg/ml, P2 contained semen sample + egg yolk tris diluent + vitamin E 1 mg/ml, P3 contained semen sample + egg yolk tris diluent + vitamin C 0,9 mg/ml + vitamin E 1 mg/ ml. The least decrease of spermatozoa motility, viability and membrane integrity was found in P3, which was significantly different to P0 (p&amp;lt;0,05). However, P1 and P2 did not show significant difference in the results of motility and viability evaluation (p&amp;gt;0,05). It can be concluded that the combination of vitamin C and E supplementation can be an optimal antioxidants supplement in egg yolk tris diluent on the quality of Sapera goat spermatozoa in 5˚C cooling process.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">661</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Amung Logam Saputro&lt;sup&gt;2,5,*&lt;/sup&gt;, Uliy Ba’sin Syadid&lt;sup&gt;1&lt;/sup&gt;, Rimayanti&lt;sup&gt;3&lt;/sup&gt;, Suherni Susilowati&lt;sup&gt;3&lt;/sup&gt;, Ragil Angga Prastiya&lt;sup&gt;3&lt;/sup&gt;, Bodhi Agustono&lt;sup&gt;4&lt;/sup&gt;, Fauzan Mumtazi&lt;sup&gt;2,5,&lt;/sup&gt; Marifatunnisa’romadhona&lt;sup&gt;2,5&lt;/sup&gt;, Anastasya&lt;sup&gt;2,5,&lt;/sup&gt; Muhammad Riesta Farhan&lt;sup&gt;2,5&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Bachelor of Veterinary Medicine, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Division of Veterinary Clinic, Department of Veterinary Clinic, Faculty of Veterinary Medicine, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Veterinary Reproduction, Faculty of Veterinary Medicine, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Animal Nutrition, Faculty of Veterinary Medicine, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Veterinary Clinic, School of Health and Life Sciences, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;
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