

Study with the several resources on Docsity
Earn points by helping other students or get them with a premium plan
Prepare for your exams
Study with the several resources on Docsity
Earn points to download
Earn points by helping other students or get them with a premium plan
Just an old cheat sheet from long ago that I had, useful for some maybe
Typology: Cheat Sheet
1 / 3
This page cannot be seen from the preview
Don't miss anything!


Preformation theory proposes that the only male and female is responsible for heredity. The male gamete consists of a miniature figure of man’s body called as homunculus which is responsible for heredity. Epigenesis (C.f.wolf
(1733-1794) and K.E. Von Baer (1792-1876) said that the
different organs and tissues of adult plant and animals developed from the uniform embryonic tissue and not from
mere growth expansion of the miniature homunculi present in eggs / sperms. Von Baer proposed that they developed
through a sequential modification of the embryonic tissue. This concept is universally accepted.
Mendel’s laws
This is also called Mendel’s first law of inheritance. According to the law of dominance, hybrid offspring will only inherit the dominant trait in the phenotype. The alleles that are suppressed are called the recessive traits while the alleles that determine the trait are known as the dominant traits.
The law of segregation states that during the production of gametes, two copies of each hereditary factor segregate so that offspring acquire one factor from each parent. In other words, allele (alternative form of the gene) pairs segregate during the formation of gamete and re-unite randomly during fertilization. This is also known as Mendel’s third law of inheritance.
Also known as Mendel’s second law of inheritance, the law of independent assortment states that a pair of traits segregates independently of another pair during gamete formation. As the individual heredity factors assort independently, different traits get equal opportunity to occur together.
Sanger sequencing begins by separating the double-stranded DNA fragments into two single-stranded DNA fragments
(denaturation). Then, an oligonucleotide primer (also known as a sequencing primer) binds to the single-stranded DNA based
on complementarity between the primer and the DNA sequence.
Next, a mixture of dNTPs and ddNTPs is added by DNA polymerase. If a dNTP is added, extension continues. If a
chain-terminating nucleotide (ddNTPs) is added, extension stops.
Because the polymerase incorporates chain-terminating nucleotides at random throughout the process, the resulting DNA
fragments at the end of the reaction vary in length. Each ddNTP also includes a different fluorescent marker, which helps in the
visualization step.