Turn the revolving turret (2) so that the lowest power objective lens (eg. 4x) is clicked into position.
Place the microscope slide on the stage (6) and fasten it with the stage clips.
Look at the objective lens (3) and the stage from the side and turn the focus knob (4) so the stage moves upward. Move it up as far as it will go without letting the objective touch the coverslip.
Look through the eyepiece (1) and move the focus knob until the image comes into focus.
Adjust the condenser (7) and light intensity for the greatest amount of light.
Move the microscope slide around until the sample is in the centre of the field of view (what you see).
Use the focus knob (4) to place the sample into focus and readjust the condenser (7) and light intensity for the clearest image (with low power objectives you might need to reduce the light intensity or shut the condenser).
When you have a clear image of your sample with the lowest power objective, you can change to the next objective lenses. You might need to readjust the sample into focus and/or readjust the condenser and light intensity. If you cannot focus on your specimen, repeat steps 3 through 5 with the higher power objective lens in place. Do not let the objective lens touch the slide!
When finished, lower the stage, click the low power lens into position and remove the slide.
Your microscope slide should be prepared with a coverslip over the sample to protect the objective lenses if they touch the slide.
Do not touch the glass part of the lenses with your fingers. Use only special lens paper to clean the lenses.
Always keep your microscope covered when not in use.
Always carry a microscope with both hands. Grasp the arm with one hand and place the other hand under the base for support.
Answer:
in the epicenter
Explanation:
In a Venn Diagram that compares and contrasts the different characteristics or features of the produced plants, "cloning" would be in the epicenter. This is because through the process of "cloning" you are basically copying the core genetic makeup of the plant and creating a brand new plant that shares all of the exact same characteristics and features as the plant's whose genetic makeup was used as a baseline.
The differences will be in:
Magnification (how zoomed-in things can be seen).
Colour (depending on the quality of the microscope colours can be seen more realistic or not).
Resolution (images can be viewed with more detail and clarity depending on the microscope).
Hope it helped,
BioTeacher101
A
Explanation:
The genome of prokaryotes has no introns hence their mRNA does not need splicing like in eukaryotic cells. Also, because the genome of prokaryotes is not delimited from the cytoplasm by a nuclear membrane, ribosomes can attach to the elongating mRNA during transcription and begin translation. Therefore translation of mRNA occurs concurrently with transcription which cannot happen with eukaryotic cells.
In the nucleus of eukaryotic cells, transcription results to a nascent mRNA which is spliced into a mature mRNA.The mature mRNA has to travel outside the nucleus to the cytoplasm to be translated by ribosomes.
Learn More:
brainly.com/question/11655383
brainly.com/question/13276299
brainly.com/question/13551177
brainly.com/question/11515691
#LearnWithBrainly
Answer:
1. Verdadero
2. Falso
3. Falso
4. Falso
5. Verdadero
Explanation:
Los seres humanos, como así también la mayoría de los mamíferos, poseen dos cromosomas sexuales: un cromosoma X y un cromosoma Y. Las hembras poseen 2 cromosomas X (un cromosoma X es heredado de la madre y el otro cromosoma X es heredado del padre); mientras que los hombres tienen un cromosoma X y un cromosoma Y (el cromosoma X es heredado de la madre, mientras que el cromosoma Y es heredado del padre). La hemofilia es una enfermedad recesiva monogénica ligada al cromosoma X, la cual está caracterizada por cuadros hemorrágicos causados por el déficit parcial y/o total de factores de coagulación. Los hombres expresan el fenotipo recesivo con mayor frecuencia que las mujeres para aquellos genes que se encuentran en el cromosoma X y poseen un mecanismo de herencia recesivo, esto debido a que los hombres sólo poseen una copia del alelo ligado al X (lo que hace que el alelo recesivo se exprese con mayor frecuencia en el fenotipo). De este modo, los hombres manifiestan hemofilia con mayor frecuencia que las mujeres porque en mujeres el gen recesivo necesita la presencia de dos copias del alelo defectuoso recesivo para que se exprese en el fenotipo hemofílico (es decir, las mujeres heterocigotas son portadoras de un alelo defectuoso pero no expresan la condición en el fenotipo), mientras que en los hombres la presencia de un sólo alelo defectuoso localizado en su único cromosoma X es suficiente para la expresión del fenotipo recesivo. En hombres, los genes ligados al cromosoma X son siempre heredados de la madre (los hombres heredan del padre el cromosoma Y). Finalmente, la herencia de caracteres ligados al cromosoma Y es muy rara porque los genes localizados en la región diferencial del cromosoma Y son escasos y estos genes solamente pueden ser trasmitidos de padres a hijos varones (ya que se encuentran en el cromosoma Y).
