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<title>BS Biology Theses</title>
<link>http://dspace.cas.upm.edu.ph:8080/xmlui/handle/123456789/170</link>
<description>Bachelor thesis of BS Biology students</description>
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<rdf:li rdf:resource="http://dspace.cas.upm.edu.ph:8080/xmlui/handle/123456789/3591"/>
<rdf:li rdf:resource="http://dspace.cas.upm.edu.ph:8080/xmlui/handle/123456789/3588"/>
<rdf:li rdf:resource="http://dspace.cas.upm.edu.ph:8080/xmlui/handle/123456789/3582"/>
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<dc:date>2026-04-12T21:59:57Z</dc:date>
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<item rdf:about="http://dspace.cas.upm.edu.ph:8080/xmlui/handle/123456789/3591">
<title>Partial Purification and Characterization of Phenoloxidase in Coconut Beetle Larvae (Oryctes rhinoceros L.)</title>
<link>http://dspace.cas.upm.edu.ph:8080/xmlui/handle/123456789/3591</link>
<description>Partial Purification and Characterization of Phenoloxidase in Coconut Beetle Larvae (Oryctes rhinoceros L.)
Umali, Janice; Yao, Jocelyn
Coconut beetle larvae have a protein called&#13;
phenoloxidase present in their hemolymph that is&#13;
essential in arthropod immune response. Prior to&#13;
characterization and isolation of an enzyme designing&#13;
optimum assay conditions is crucial. This will stabilize&#13;
the enzyme and ensure optimal activity. In this study,&#13;
phenoloxidase activity was measured as a function of&#13;
varying substrates, activators with their incubation&#13;
periods and incubation temperatures, and buffer pH. The&#13;
substrate 4-methylcatechol appeared as the best substrate&#13;
for the enzyme. Among the activators tested, trypsin&#13;
efficiently activated phenoloxidase within 20-60 minutes&#13;
incubation periods at 30°C in sodium phosphate buffer&#13;
with pH ranging from 6.0 to 8.0. The hemolymph was&#13;
partially purified for pro-phenoloxidase through DEAE&#13;
and SP ion-exchange chromatography. Fractions positive&#13;
for enzyme activity were loaded on SOS-PAGE. Partially&#13;
purified prophenoloxidase shows a molecular weight of&#13;
85-92 kDa while its active form (phenoloxidase) has a&#13;
molecular weight of 62-67 kDa.
</description>
<dc:date>2002-03-01T00:00:00Z</dc:date>
</item>
<item rdf:about="http://dspace.cas.upm.edu.ph:8080/xmlui/handle/123456789/3588">
<title>A Study on the Meristic and Morphometric Characteristics of Thailand Strain and GIFT Strain of Nile Tilapia (Oreochromis niloticus)</title>
<link>http://dspace.cas.upm.edu.ph:8080/xmlui/handle/123456789/3588</link>
<description>A Study on the Meristic and Morphometric Characteristics of Thailand Strain and GIFT Strain of Nile Tilapia (Oreochromis niloticus)
Veto, Rholine Gem Martin S.; Tismal, Daniel S. II
Thirteen biometric characters were used to differentiate and&#13;
compare the Thailand-strain and the GIFT-strain of Nile Tilapia&#13;
(Oreochromis niloticus). Meristic and morphometric data from 30&#13;
samples for each strain were subjected to descriptive and statistical&#13;
analysis. The study showed that there are no significant differences in all&#13;
meristic characters (number of dorsal fin rays, number of pectoral fin rays,&#13;
number of pelvic fin rays, and number or anal fin rays) as well as the&#13;
horizontal eye diameter between the Thailand-strain and GIFT-strain of 0.&#13;
niloticus. Generally, the GIFT-strain of 0. niloticus has greater values for&#13;
the other morphometric characters (head length, preorbital distance,&#13;
postorbital distance, orbital depth or the head, occipital depth of the head,&#13;
total body length, standard length, and total body weight) compared to the&#13;
Thailand-strain 0. niloticus
</description>
<dc:date>2002-02-01T00:00:00Z</dc:date>
</item>
<item rdf:about="http://dspace.cas.upm.edu.ph:8080/xmlui/handle/123456789/3582">
<title>Effects of Cyclooxygenase Inhibitors on the Radiation Response of Intestinal Crypt Cells in Male Mice</title>
<link>http://dspace.cas.upm.edu.ph:8080/xmlui/handle/123456789/3582</link>
<description>Effects of Cyclooxygenase Inhibitors on the Radiation Response of Intestinal Crypt Cells in Male Mice
Dones, Rosa Angela SA.; Serna, Paulene-Ver A.
The effects of varying doses of different types of&#13;
Cyclooxygenase (COX) inhibitors on irradiated and nonirradiated&#13;
murine intestinal crypt cells were investigated.&#13;
Cell counts, supported by data from TUNEL assay and&#13;
immunohistochemical analyses, revealed that apoptosis was&#13;
greatest in irradiated tissues treated with NSAIDS.&#13;
Irradiated cells treated with COX-2 inhibitors showed least&#13;
occurrence of apoptosis with increased occurrence of&#13;
regenerating cells. Results suggest a potential role of COX-&#13;
2 selective inhibitors as a radioprotective agent for normal&#13;
cells in radiation therapy.
</description>
<dc:date>2002-03-01T00:00:00Z</dc:date>
</item>
<item rdf:about="http://dspace.cas.upm.edu.ph:8080/xmlui/handle/123456789/3581">
<title>The Radioprotective Effects of Glo-Herbal on the Bone Marrow of Irradiated Albino Mice (Mus musculus L.)</title>
<link>http://dspace.cas.upm.edu.ph:8080/xmlui/handle/123456789/3581</link>
<description>The Radioprotective Effects of Glo-Herbal on the Bone Marrow of Irradiated Albino Mice (Mus musculus L.)
Dela Cruz, Aileen; Yuhico, Luke
The radioprotective effect of Glo-Herbal was demonstrated using the&#13;
micronucleus test. Four 7-week old mice (Mus musculus L.) were used for&#13;
each of the six groups: negative control group, positive control group,&#13;
25%, 50%, 75% and 100% treatment groups. The negative control group&#13;
. Was not given any treatment nor exposed to radiation, while the positive&#13;
control group was not given any treatment but was exposed to radiation.&#13;
The concentrations were administered ad libitum via drinking bottles, for&#13;
30 days. Ionizing gamma radiation (6Gy) was used to induce formation of&#13;
micronucleus on the bone marrow cells of the mice. The mice sacrificed&#13;
and the femori were extracted. The bone marrow cells were collected for&#13;
slide preparation. One thousand polychromatic erythrocytes (PCEs) per&#13;
mouse were screened. The mean frequencies of micro nucleated&#13;
polychromatic erythrocytes were as follows: 36.5 +/-5.5 (positive control),&#13;
20.25 +/-4.75 (25% treatment group), 15 +/-3.5 (50% treatment group),&#13;
14.25 +/-0.875 (75% treatment group), 12 +/-2.0 (100% treatment group)&#13;
and 7.5 +/-2.0 (negative control). Using the Kruskal-Wallis one way&#13;
ANOVA, it was proven that the groups’ responses varied. Multiple&#13;
comparisons procedure showed that there is a significant difference only&#13;
between the positive and negative control group. This indicates that the&#13;
effects of Glo-Herbal follow a dose-dependent pattern, but are not great&#13;
enough to be considered statistically significant.
</description>
<dc:date>2002-03-01T00:00:00Z</dc:date>
</item>
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