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HEXA cDNA Clone – Hexosaminidase A (Alpha Polypeptide) (Human)

For Research Use Only. Not for use in diagnostic procedures. Catalog #: MBS1265985

MBS1265985 is a cDNA clone targeting HEXA. More details

$400 / 0.01 mg Plasmid + 0.2 mL Glycerol-Stock +1 FREE 8GB USB
Product Documentation
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Sample Manual Insert View PDF
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Testing Data View PDF
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Certificate of Analysis (COA) View PDF
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QC Report View PDF
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Material Safety Data Sheet View PDF
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Technical Datasheet View PDF
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Protocol View PDF

Product Overview

Online Datasheet in PDF
Product Name
HEXA, cDNA Clone
Full Product Name
HEXA cDNA Clone
Product Gene Name
Sequence
atgacaagtt ccaggctttg gttttcgctg ctgctggcgg cagcgttcgc aggacgggcg acggccctct ggccctggcc tcagaacttc caaacctccg accagcgcta cgtcctttac ccgaacaact ttcaattcca gtacgatgtc agctcggccg cgcagcccgg ctgctcagtc ctcgacgagg ccttccagcg ctatcgtgac ctgcttttcg gttccgggtc ttggccccgt ccttacctca cagggaaacg gcatacactg gagaagaatg tgttggttgt ctctgtagtc acacctggat gtaaccagct tcctactttg gagtcagtgg agaattatac cctgaccata aatgatgacc agtgtttact cctctctgag actgtctggg gagctctccg aggtctggag acttttagcc agcttgtttg gaaatctgct gagggcacat tctttatcaa caagactgag attgaggact ttccccgctt tcctcaccgg ggcttgctgt tggatacatc tcgccattac ctgccactct ctagcatcct ggacactctg gatgtcatgg cgtacaataa attgaacgtg ttccactggc atctggtaga tgatccttcc ttcccatatg agagcttcac ttttccagag ctcatgagaa aggggtccta caaccctgtc acccacatct acacagcaca ggatgtgaag gaggtcattg aatacgcacg gctccggggt atccgtgtgc ttgcagagtt tgacactcct ggccacactt tgtcctgggg accaggtatc cctggattac tgactccttg ctactctggg tctgagccct ctggcacctt tggaccagtg aatcccagtc tcaataatac ctatgagttc atgagcacat tcttcttaga agtcagctct gtcttcccag atttttatct tcatcttgga ggagatgagg ttgatttcac ctgctggaag tccaacccag agatccagga ctttatgagg aagaaaggct tcggtgagga cttcaagcag ctggagtcct tctacatcca gacgctgctg gacatcgtct cttcttatgg caagggctat gtggtgtggc aggaggtgtt tgataataaa gtaaagattc agccagacac aatcatacag gtgtggcgag aggatattcc agtgaactat atgaaggagc tggaactggt caccaaggcc ggcttccggg cccttctctc tgccccctgg tacctgaacc gtatatccta tggccctgac tggaaggatt tctacgtagt ggaacccctg gcatttgaag gtacccctga gcagaaggct ctggtgattg gtggagaggc ttgtatgtgg ggagaatatg tggacaacac aaacctggtc cccaggctct ggcccagagc aggggctgtt gccgaaaggc tgtggagcaa caagttgaca tctgacctga catttgccta tgaacgtttg tcacacttcc gctgtgagtt gctgaggcga ggtgtccagg cccaacccct caatgtaggc ttctgtgagc aggagtttga acagacctga
Molecular Weight
19,326 Da
OMIM
272800
Vector
pUC
Clone Sequence Report
Provided with product shipment
ISO Certification
Manufactured in an ISO 9001:2015 Certified Laboratory.

Other Notes

Small volumes of HEXA cdna clone vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.

Additional Details

NCBI/Uniprot data below describe general gene information for HEXA. It may not necessarily be applicable to this product.

NCBI GI #
NCBI GeneID
NCBI Accession #
UniProt Secondary Accession #
UniProt Related Accession #
NCBI Official Full Name
Homo sapiens hexosaminidase A (alpha polypeptide), mRNA
NCBI Official Synonym Full Names
hexosaminidase subunit alpha
NCBI Official Symbol
HEXA
NCBI Official Synonym Symbols
TSD
UniProt Protein Name
Beta-hexosaminidase subunit alpha
UniProt Synonym Protein Names
Beta-N-acetylhexosaminidase subunit alpha; Hexosaminidase subunit A; N-acetyl-beta-glucosaminidase subunit alpha
Protein Family
UniProt Gene Name
HEXA
UniProt Synonym Gene Names
Hexosaminidase subunit A
UniProt Entry Name
HEXA_HUMAN
NCBI Protein Information
beta-hexosaminidase subunit alpha

NCBI Summary for HEXA

This gene encodes a member of the glycosyl hydrolase 20 family of proteins. The encoded preproprotein is proteolytically processed to generate the alpha subunit of the lysosomal enzyme beta-hexosaminidase. This enzyme, together with the cofactor GM2 activator protein, catalyzes the degradation of the ganglioside GM2, and other molecules containing terminal N-acetyl hexosamines. Mutations in this gene lead to an accumulation of GM2 ganglioside in neurons, the underlying cause of neurodegenerative disorders termed the GM2 gangliosidoses, including Tay-Sachs disease (GM2-gangliosidosis type I). Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed. [provided by RefSeq, Jan 2016]
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UniProt Comments for HEXA

HEXA: Responsible for the degradation of GM2 gangliosides, and a variety of other molecules containing terminal N-acetyl hexosamines, in the brain and other tissues. The form B is active against certain oligosaccharides. The form S has no measurable activity. Defects in HEXA are the cause of GM2-gangliosidosis type 1 (GM2G1); also known as Tay-Sachs disease. GM2- gangliosidosis is an autosomal recessive lysosomal storage disease marked by the accumulation of GM2 gangliosides in the neuronal cells. GM2G1 is characterized by GM2 gangliosides accumulation in the absence of HEXA activity, leading to neurodegeneration and, in the infantile form, death in early childhood. GM2G1 has an increased incidence among Ashkenazi Jews and French Canadians in eastern Quebec. It exists in several forms: infantile (most common and most severe), juvenile and adult (late onset). Belongs to the glycosyl hydrolase 20 family.

Protein type: Glycan Metabolism - glycosphingolipid biosynthesis - globo series; Carbohydrate Metabolism - amino sugar and nucleotide sugar; Hydrolase; Glycan Metabolism - glycosaminoglycan degradation; EC 3.2.1.52; Glycan Metabolism - other glycan degradation; Glycan Metabolism - glycosphingolipid biosynthesis - ganglio series

Chromosomal Location of Human Ortholog: 15q24.1

Cellular Component: azurophil granule; lysosomal lumen; membrane

Molecular Function: acetylglucosaminyltransferase activity; beta-N-acetylhexosaminidase activity; protein heterodimerization activity

Biological Process: chondroitin sulfate catabolic process; glycosaminoglycan biosynthetic process; glycosphingolipid metabolic process; hyaluronan catabolic process; keratan sulfate catabolic process

Disease: Tay-sachs Disease
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Precautions

All of MyBioSource's Products are for scientific laboratory research purposes and are not for diagnostic, therapeutics, prophylactic or in vivo use. Through your purchase, you expressly represent and warrant to MyBioSource that you will properly test and use any Products purchased from MyBioSource in accordance with industry standards. MyBioSource and its authorized distributors reserve the right to refuse to process any order where we reasonably believe that the intended use will fall outside of our acceptable guidelines.

Disclaimer

While every efforts were made to ensure the accuracy of the information provided in this datasheet, MyBioSource will not be liable for any omissions or errors contained herein. MyBioSource reserves the right to make changes to this datasheet at any time without prior notice.

It is the responsibility of the customer to report product performance issues to MyBioSource within 30 days of receipt of the product. Please visit our Terms & Conditions page for more information.

Product Note

Select online data sheet information is drawn from bioinformatics databases, occasionally resulting in ambiguous or non-relevant product information. It is the responsibility of the customer to review, verify, and evaluate the information to make sure it matches their requirements before purchasing the kit. Our ELISA Kit assays are dynamic research tools and sometimes they may be updated and improved. If the format of this assay is important to you then please request the current manual or contact our technical support team with a presales inquiry before placing an order. We will confirm the current details of the assay. We cannot guarantee the sample manual posted online is the most current manual, it is intended to serve as an example only. Please refer to the instructions For Use provided with the assay kit for precise details.

Product PubMed Publications

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