Amelogenin locus is used for gender identification. Why?
Amelogenin is a group of closely related protein involved in enamel development, a process known as amelogenesis. A single copy of amelogenin gene is located on both X and Y chromosomes at Xp22.1-Xp22.3 and Yp11.2 locus. Amelogenin gene is present in non-recombining region of Y chromosome.The gene exists in different versions on X and Y chromosomes. Intron 1 of amelogenin gene has a 6 bp deletion in X chromosome while there is no deletion in intron 1 in amelogenin gene version present on Y chromosome.This difference in amelogenin locus on X and Y chromosomes helps in gender identification of unknown human samples. Gel electrophoresis resulting in two bands of DNA at 555 bp and 371 bp indicates both X and Y version of amelogenin gene thus confirming the gender to be male whereas only one band of DNA at 555 bp indicates only X version of amelogenin gene thus confirming the gender to be female.
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The table shown relates political party identification and gender POLITICAL PARTY IDENTIFICATION GENDER Democrat Independent Republican Total 1567 1229 Females Males 158 105 835 735 574 389 a. ldentify the response variable and the explanatory variable. Gender is the explanatory variable. Political party identification is the b. Construct a table showing the conditional distributions of the response variable. Interpret. variable. POLITICAL PARTY IDENTIFICATION GENDER Democrat Independent Republican Total Females 5.7%...
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Explain why every time we find a specific allele of a polymorphic locus (say, for Locus 32>allele type 4) in humans it is embedded within a haplotype that contains specific alleles of polymorphic loci that flank that locus (say Locus 31>allele type 2 and Locus 33>allele type 3). In this example, assume 6 different alleles for each locus have been found within the whole human population. Our haplotype example shown below: 31 32 33 (type 2) (type 4) (type3) Locus.........
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1.1.15-Gender Selection in a study of the Gender Aide method of gender selection used to 980 boys and 1020 girls. There is about a 19% chance of getting that many girls if the significance, but method had no e¥ect. a tohle what inuo pobo addressed by
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3. Explain why every time we find a specific allele of a polymorphic locus in humans it is embedded within a haplotype that contains specific alleles of polymorphic loci that flank that locus. For example, three adjacent loci (Locus 31, Locus 32, and Locus 33) are all polymorphic and each locus has 6 different alleles found within the whole human population. Why do we tend to see specific combinations of alleles together at these three loci (e.g. the type 2...
1. What is the source of the “spacer” DNA in the bacterial CRISPR locus? 2. Why does the cas9 enzyme have two nuclease domains? 3. What is the relationship between the tracrRNA and the regularly interspersed repeats of the CRISPR locus? Why is this important? 4. In the lab version of the CRISPR/cas9 system, what is the “chimeric RNA”?