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SPG20 cDNA Clone – Spastic Paraplegia 20 (Troyer Syndrome) (Human)

For Research Use Only. Not for use in diagnostic procedures. Catalog #: MBS1269871

MBS1269871 is a cDNA clone targeting SPG20. More details

$520 / 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
SPG20, cDNA Clone
Full Product Name
SPG20 cDNA Clone
Product Gene Name
Sequence
atggagcaag agccacaaaa tggagaacct gctgaaatta agatcatcag agaagcatat aagaaggcct ttttatttgt taacaaaggt ctgaatacag atgaattagg tcagaaggaa gaagcaaaga actactataa gcaaggaata ggacacctgc tcagagggat cagcatttca tcaaaagagt ctgaacacac aggtactggg tgggaatctg ctagacagat gcaacagaaa atgaaagaaa ctctacagaa tgtacgcacc aggctggaaa ttctagagaa gggtcttgcc acttctctgc agaatgatct tcaggaggtg cccaagttat atccagaatt tccacctaaa gacatgtgtg aaaaattacc agagcctcag tcttttagtt cagctcctca gcatgctgaa gtaaatggaa acacctcaac tccaagtgca ggggcagttg ctgcacctgc ttctctgtct ttaccatcac aaagttgtcc agcagaagct cctcctgctt atactcctca agctgctgaa ggtcactaca ctgtatccta tggaacagat tctggggagt tttcatcagt tggagaggag ttttatagga atcattctca gccaccgcct cttgagacct tagggctgga tgcagatgaa ttgattttga taccaaatgg agtacagatt ttttttgtaa atcctgcagg ggaggttagt gcaccttcgt atcctgggta ccttcgaatt gtgaggtttt tggataattc tctcgatacg gttctaaacc gtcctcccgg gtttcttcag gtttgtgact ggttatatcc tctagttcct gatagatctc cggttctgaa atgtactgcg ggagcctaca tgtttcctga tacaatgcta caagcagcag gatgctttgt gggggtcgtc ctgtcctctg agttaccaga ggatgataga gagctctttg aggatctgtt aaggcaaatg tctgaccttc ggctccaggc caactggaac agagcagaag aagaaaatga attccaaatc cctggaagaa ctagaccctc ctctgaccaa ctaaaagaag cctctggcac tgatgtgaaa cagttggacc aaggcaataa ggatgtacgt cataaaggaa aacgtggaaa aagggctaaa gatacttcaa gtgaagaagt taacctgagt cacattgtac catgtgagcc agttccagaa gaaaagccaa aagaattaca tgaatggagt gaaaaagtgg ctcacaacat tttgtcaggt gcttcctggg tgagttgggg tttagtcaaa ggtgctgaga ttactggtaa ggcaatccag aaaggtgctt ctaaactccg agagcggatt caaccagaag aaaaacccgt ggaagttagt ccagctgtca ccaagggact ttatatagcg aagcaagcta caggaggagc agcaaaagtc agtcagttcc tggttgatgg agtttgcact gtagcaaatt gcgttggaaa agaactagct ccacatgtca agaagcatgg aagcaaactt gttccagaat ctcttaaaaa agacaaagat gggaaatctc ctctggatgg tgctatggtt gtagcagcga gtagtgttca aggattttca actgtctggc aaggattgga atgtgcagct aaatgcatcg ttaacaatgt ttcagcagaa actgtacaaa ctgtcagata caaatacgga tataatgcag gagaagctac ccaccatgcg gtggattctg cggtcaatgt tggcgtaact gcctacaata ttaacaacat tggtatcaaa gcaatggtga agaaaactgc aacacaaaca ggacacactc tccttgagga ctatcagata gttgataatt ctcagaggga aaatcaagaa ggagcagcaa atgtcaacgt gagaggggag aaggatgagc agacgaagga agtaaaggag gcaaagaaga aagataaatg a
Molecular Weight
72,833 Da
OMIM
275900
Vector
pENTR223.1 or pUC
Clone Sequence Report
Provided with product shipment
ISO Certification
Manufactured in an ISO 9001:2015 Certified Laboratory.

Other Notes

Small volumes of SPG20 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 SPG20. 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 spastic paraplegia 20 (Troyer syndrome), mRNA
NCBI Official Synonym Full Names
spastic paraplegia 20 (Troyer syndrome)
NCBI Official Symbol
SPG20
NCBI Official Synonym Symbols
SPARTIN; TAHCCP1
UniProt Protein Name
Spartin
UniProt Synonym Protein Names
Spastic paraplegia 20 protein; Trans-activated by hepatitis C virus core protein 1
Protein Family
UniProt Gene Name
SPG20
UniProt Synonym Gene Names
KIAA0610; TAHCCP1
UniProt Entry Name
SPG20_HUMAN
NCBI Protein Information
spartin

NCBI Summary for SPG20

This gene encodes a protein containing a MIT (Microtubule Interacting and Trafficking molecule) domain, and is implicated in regulating endosomal trafficking and mitochondria function. The protein localizes to mitochondria and partially co-localizes with microtubules. Stimulation with epidermal growth factor (EGF) results in protein translocation to the plasma membrane, and the protein functions in the degradation and intracellular trafficking of EGF receptor. Multiple alternatively spliced variants, encoding the same protein, have been identified. Mutations associated with this gene cause autosomal recessive spastic paraplegia 20 (Troyer syndrome). [provided by RefSeq, Nov 2008]
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UniProt Comments for SPG20

SPG20: May be implicated in endosomal trafficking, or microtubule dynamics, or both. Defects in SPG20 are the cause of spastic paraplegia autosomal recessive type 20 (SPG20); also known as Troyer syndrome (TRS). Spastic paraplegia is a neurodegenerative disorder characterized by a slow, gradual, progressive weakness and spasticity of the lower limbs. Rate of progression and the severity of symptoms are quite variable. Initial symptoms may include difficulty with balance, weakness and stiffness in the legs, muscle spasms, and dragging the toes when walking. In some forms of the disorder, bladder symptoms (such as incontinence) may appear, or the weakness and stiffness may spread to other parts of the body. SPG20 is characterized by dysarthria, distal amyotrophy, mild developmental delay and short stature.

Protein type: Unknown function

Chromosomal Location of Human Ortholog: 13q13.3

Cellular Component: cytoplasm; midbody; mitochondrial outer membrane; plasma membrane

Molecular Function: protein binding; ubiquitin protein ligase binding

Biological Process: abscission; cell division; regulation of mitochondrial membrane potential

Disease: Spastic Paraplegia 20, Autosomal Recessive
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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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