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当前位置: 首页 > 产品中心 > > Bioclone/BcMag™ Rootless Hair DNA Purification Kit/100x preps/AD102
商品详细Bioclone/BcMag™ Rootless Hair DNA Purification Kit/100x preps/AD102
Bioclone/BcMag™ Rootless Hair DNA Purification Kit/100x preps/AD102
Bioclone/BcMag™ Rootless Hair DNA Purification Kit/100x preps/AD102
商品编号: AD102
品牌: Bioclone Inc
市场价: ¥9000.00
美元价: 5400.00
产地: 美国(厂家直采)
公司:
产品分类: 其他
公司分类:
联系Q Q: 3392242852
电话号码: 4000-520-616
电子邮箱: info@ebiomall.com
商品介绍

The Significance of Hair in Forensics and Medical Research

Hair is one of the most commonly found evidence at crime scenes and is gaining importance as a sample type for medical research inquiries. In criminology, hair has been used for population-based statistical analysis and DNA-based analysis. DNA testing using hair samples is most valuable when a short repeat analysis of nuclear DNA (nuDNA) is performed and the hair’s root and adherent tissue are present.

Advantages of Hair in Genetic Genealogy

Rootless hair has distinct advantages in forensic circumstances. Hair is insoluble, preserving DNA for centuries, and the extracted DNA is less susceptible to microbial contamination than bone and teeth samples. Moreover, a single hair is a distinct biological entity, which eliminates the concern of sample mix-ups in DNA-based forensics studies.

The Structure of Hair and its DNA

The hair follicle and hair shaft are the two sections of hair from which DNA can be extracted and purified. The hair follicle can isolate cellular DNA (nuDNA) and mitochondrial DNA (mtDNA), while the hair shaft often contains mtDNA and may have little nuclear material. Shed hair, which accounts for up to 90% of hair samples obtained at crime scenes, undergoes keratinization, stiffening, and nucleus breakdown. On the other hand, unwashed hair has a higher DNA output due to surrounding cells adhering to the hair shafts, which can be a source of nuDNA. Although some nuclear DNA is known to remain in rootless hair shafts, it is in small quantities and of highly varied quality.

Mitochondrial DNA Sequencing

MtDNA analysis can be used to connect human hair to a suspect. Unlike nuDNA, mtDNA lacks selective potential due to its ubiquity within the maternal lineage, making it difficult to differentiate between a grandmother and her daughter or grandchildren. MtDNA sequencing can also provide important information in species identification, as not all hair samples are human.

Nuclear DNA for Short Tandem Repeat (STR) Typing

Forensic laboratories usually examine hair evidence for the presence of root material before processing it. If the sample lacks root material, it is frequently not processed or sent for mtDNA sequencing, which has historically proven more successful than nuDNA on hair shafts. However, recent studies have shown that despite being fragmented, nuclear DNA can be retrieved from shed hair, and it accounts for most of the total DNA, eliminating the assumption that only mtDNA can be recovered from rootless hair. This method has enabled the characterization of nuDNA in telogen hairs that would not have been achievable using conventional techniques.

Optimizing DNA Extraction from Hair Shafts

DNA extraction is the first step in the forensic analysis of rootless hair. To extract ultrashort DNA from a single rootless hair, it is critical to optimize the settings to maximize the yield and purity of DNA collected from diverse samples using various procedures. A streamlined method for extracting DNA from hair shafts eliminates DNA contamination while reducing analysis time, making it valuable to the forensic and population-based research communities. The BcMag™ Rootless Hair DNA Purification Kit is designed to extract pigment-free nucleic acids from single rootless hair efficiently and sequentially, using magnetic beads and an optimized demineralization buffer to yield high-quality DNA. The purified genomic DNA has the highest integrity and can be used in various downstream applications such as qPCR, STR, etc.

Hair-Pigment-Removal.png

Workflow of Hair Shaft DNA purification and Results

1.

Lyse the hair at 95°C for 2 hours.

2.

Add magnetic beads to bind the DNA.

3.

Wash the beads.

4.

Elute DNA from the beads.

Workflow of Hair Shaft DNA purification

Learn More

Instruction Manual

MSDS

DNA & RNA Purification Related Products →

General Reference

1.

Brandhagen MD, Loreille O, Irwin JA. Fragmented Nuclear DNA Is the Predominant Genetic Material in Human Hair Shafts. Genes. 2018 Dec;9(12):640.

2.

Melton T, Holland C. Routine forensic use of the mitochondrial 12S ribosomal RNA gene for species identification. Journal of forensic sciences. 2007 Nov;52(6):1305-7.

3.

Luo S, Valencia CA, Zhang J, Lee NC, Slone J, Gui B, Wang X, Li Z, Dell S, Brown J, Chen SM. Biparental inheritance of mitochondrial DNA in humans. Proceedings of the National Academy of Sciences. 2018 Dec 18;115(51):13039-44.

4.

Opel KL, Fleishaker EL, Nicklas JA, Buel E, McCord BR. Evaluation and quantification of nuclear DNA from human telogen hairs. Journal of forensic sciences. 2008 Jul;53(4):853-7.

5.

Brown H, Thompson R, Murphy G, Peters D, La Rue B, King J, Montgomery AH, Carroll M, Baus J, Sinha S, Wendt FR. Development and validation of a novel multiplexed DNA analysis system, InnoTyper® 21. Forensic Science International: Genetics. 2017 Jul 1;29:80-99.

6.

Grisedale KS, Murphy GM, Brown H, Wilson MR, Sinha SK. Successful nuclear DNA profiling of rootless hair shafts: a novel approach. International journal of legal medicine. 2018 Jan 1;132(1):107-15.

7.

Brandhagen MD, Loreille O, Irwin JA. Fragmented Nuclear DNA Is the Predominant Genetic Material in Human Hair Shafts. Genes. 2018 Dec;9(12):640.

8.

Parker GJ, Leppert T, Anex DS, Hilmer JK, Matsunami N, Baird L, Stevens J, Parsawar K, Durbin-Johnson BP, Rocke DM, Nelson C. Demonstration of protein-based human identification using the hair shaft proteome. PloS one. 2016 Sep 7;11(9):e0160653.

品牌介绍
Bioclone的用于学术研究和治疗应用的重组蛋白/ DNA的数量已大大增加。然而,成功的重组蛋白表达取决于许多因素,例如密码子偏好性,RNA二级结构,异源表达系统中的GC含量。越来越多的实验结果证明,与预优化相比,取决于不同的基因,表达水平显着提高,从两倍提高到一百倍。Bioclone开发了一个独特的专有技术平台,并生成了超过14,000个人工合成的,经过密码子优化的cDNA / DNA克隆(克隆在大肠杆菌表达载体中,图1)和重组蛋白(在大肠杆菌酵母中生产)。Bioclone为所有cDNA克隆和重组蛋白生产提供即用型和基于客户的服务。特别设计和合成了数十万种重组蛋白和密码子优化的cDNA (DNA开放阅读框)。  密码子优化的cDNA / DNA:    产生更高产量的重组蛋白。将cDNA / DNA 克隆克隆到具有6x His -tag的大肠杆菌表达载体中,可立即用于重组蛋白生产。可以使用作为验证的RNAi的功能由于在其〜30%差的RNAi的援助cDNA序列时相比原的cDNA / DNA 。Bioclone 还提供客户服务克隆中的cDNA插入NY 所需的客户向量小号。重组蛋白:重组蛋白C 在N末端或C末端具有6x His-tag重组蛋白P roduced在大肠杆菌或小号F9昆虫细胞。  provid 我纳克准备使用的重组蛋白和p rotein点播服务的所有cDNA克隆。通过SDS-PAGE 测定的重组蛋白纯度> 90%。ř ecombinant蛋白应用:Western印迹,ELISA 或可以用于其它应用。  cDNA克隆和重组蛋白包括:我nfection疾病抗原(病毒,细菌,寄生虫,细菌毒素),抗过敏的蛋白质,细胞因子,   激酶,磷酸酶,信号转导,   干细胞和发展,神经科学, 药物   metabollism,普通的病,转录因子,癌症和更重组蛋白质和克隆是g 还是机翼.......