XFiling™ Kit v1.2

Cat. No: KBC-120108

X Chromosome Profile Determination Ki

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Cat. No KBC-120108 Categories: ,
Description

The KBC human identification profiling kits are used in various fields such as human identification, forensic medicine, parentage testing, kinship analysis, research, and so on.

Human identification profiling kits have been developed worldwide due to their extensive application in forensic genetics. These kits can be used to search databases and have high heterozygosity for most populations. Therefore, these kits can be used for various types of human identification, parentage testing, forensic medicine, and kinship studies. KBC HID kits are designed based on STR markers recommended by the European Network of Forensic Science Institutes (ENFSI), the National Institute of Standards and Technology (NIST), the International Society for Forensic Genetics (ISFG), and the Combined DNA Index System (CODIS).

Kawsar Biotech Company offers several HID kits for various purposes. These kits include:

  • IRFiling™ kit (with 17 markers in a 5-color system) is a preferred kit for most forensic medical cases. According to CODIS, a minimum of 13 markers is recommended for identity determination, and this kit uses 17 markers.
  • IRFiling™ Globe (with 27 markers in a 6-color system) is currently used more for forensic medical purposes worldwide, especially when the FBI introduced new CODIS markers in 2016.
  • The X chromosome-related kit called XFiling™ with 17 markers, 15 of which are specific to the X chromosome, operates in a 5-color system.
  • The Y chromosome-related kit named YFiling™ (29-Plex) with 30 markers, also in a 5-color system, can be used for criminal investigations as well as male kinship analysis.

A comparison table has been prepared for selecting the appropriate human profiling kit for forensic medical purposes and identification in line with the goals of our dear customers.

IRFiling™ Globe

kit v1.2

™IRFiling

kit v2.2

™XFiling

kit v1.2

YFiling™ (29-Plex)

Kit v2.2

Features

 

27172730Total markers

More powerful
✓✓✓Crime investigation
XPaternity/Maternity test
×XXMale to male relation Y Chr.
×XXY specific
×XXXSisters from same father X Chr.
×XXXX Specific
Ancient/bone/aged DNA
24162429STR markers
Gender determination
201520CODIS markers 2017
65655or 6 dye system
Single multiplex PCR
3500/3500xL3130/3130xl

3500/3500xL

3500/3500xL3130/3130xl

3500/3500xL

ABI GA Systems

DNA contains unique sequences of short tandem repeats (STRs) consisting of 3 to 7 base pairs scattered throughout the genome, which can be used for individual identification in forensic medicine. Since the exact number of repeats at each specific location varies among different individuals, forensic medicine can utilize these markers for identification purposes. Furthermore, each individual has two sets of STRs inherited from both parents, and each of these sets can have a different number of repeats at the same locus. In fact, a DNA profile is recognized as a DNA fingerprint that distinguishes individuals from each other and is only similar in identical twins.

The XFiling™ Kit v1.2 is used in forensic genetics, human identity determination, and kinship analysis in human female samples. This kit determines identity based on 17 markers, including 15 X-STR markers with high heterozygosity, one amelogenin marker (AMXY), and one autosomal marker (this marker is for minimizing the risk of sample mix-up). These markers are organized into 4 haplogroups. This kit can be used to differentiate female profiles, especially in forensic and kinship cases, such as determining the sororal relationship between two women in the absence of paternal alleles. It is also used to identify the genotype of a female in the background of male samples. Another application is the analysis of diseases located on the X chromosome. The advantage of this kit over similar foreign kits is having three additional loci, which increases the accuracy of the analysis. All 17 markers are amplified using the Multiplex PCR method, and the results are determined using capillary electrophoresis.

For more information about the product, its use, and result analysis, please refer to the user manual.

Features

Some applications of the kit include:

  • Determining kinship in human female samples
  • Drawing haplotype for individuals with X-linked diseases
  • Investigating crossing over in individuals with X-linked diseases
  • Determining fetal sex
  • Forensic genetics

 

This kit can be used on DNA samples extracted from blood, amniotic fluid (AF), chorionic villus samples (CVS), and DBC card (KBC DNA Banking card), blood lysing buffer (BLB), amniotic cell lysing buffer (AFL), and chorionic villus lysing buffer (CVL).

markers

Usage

Among the uses of the kit, the following can be mentioned:

  • Determination of kinship ratio in human female samples
  • Haplotype drawing for people with X-linked diseases
  • Investigation of crossing over of people with X-linked diseases
  • Determining the sex of the fetus
  • Legal genetics

This kit is used on DNA samples purified from blood, amniotic fluid (AF), chorionic villus sample (CVS) and DBC card (DNA storage card produced by Kawsar Biotech Company), BLB blood lysing buffer, amniotic cell lysing buffer. AFL, and CVL paired villus lysing buffer can be used.

To learn more about the product and how to use it, as well as to analyze the results, refer to the manual.

Compatibility

The XFiling™ v1.2 Kit is compatible with 5-dye capillary electrophoresis systems such as ABI PRISM 3130/3130xl/3500/3500xL Genetic Analyzers with capillary sizes of 30, 50, or 80 centimeters.

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