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Human NHL repeat containing 1 ELISA Kit | NHLRC1 elisa kit

Human E3 ubiquitin-protein ligase NHLRC1, NHLRC1 ELISA Kit

Gene Names
NHLRC1; EPM2A; EPM2B; MALIN; bA204B7.2
Reactivity
Human
Synonyms
NHL repeat containing 1; Human E3 ubiquitin-protein ligase NHLRC1; NHLRC1 ELISA Kit; Human E3 ubiquitin-protein ligase NHLRC1 (NHLRC1) ELISA kit; EPM2A; EPM2B; MALIN; MGC119262; MGC119264; MGC119265; bA204B7.2; epilepsy; progressive myoclonus type 2B; NHLRC1 elisa kit
Ordering
For Research Use Only!
Reactivity
Human
Preparation and Storage
Store all reagents at 2-8 degree C

NCBI and Uniprot Product Information

NCBI GI #
NCBI GeneID
NCBI Accession #
NCBI GenBank Nucleotide #
UniProt Accession #
Molecular Weight
42,293 Da
NCBI Official Full Name
E3 ubiquitin-protein ligase NHLRC1
NCBI Official Synonym Full Names
NHL repeat containing E3 ubiquitin protein ligase 1
NCBI Official Symbol
NHLRC1
NCBI Official Synonym Symbols
EPM2A; EPM2B; MALIN; bA204B7.2
NCBI Protein Information
E3 ubiquitin-protein ligase NHLRC1; NHL repeat containing 1; NHL repeat-containing protein 1
UniProt Protein Name
E3 ubiquitin-protein ligase NHLRC1
UniProt Gene Name
NHLRC1
UniProt Synonym Gene Names
EPM2B
UniProt Entry Name
NHLC1_HUMAN

NCBI Description

The protein encoded by this gene is a single subunit E3 ubiquitin ligase. Laforin is polyubiquitinated by the encoded protein. Defects in this intronless gene lead to an accumulation of laforin and onset of Lafora disease, also known as progressive myoclonic epilepsy type 2 (EPM2).[provided by RefSeq, Mar 2010]

Uniprot Description

NHLRC1: E3 ubiquitin-protein ligase which in complex with EPM2A/laforin and HSP70 suppresses the cellular toxicity of misfolded proteins by promoting their degradation through the ubiquitin-proteasome system (UPS). Ubiquitinates PPP1R3C/PTG in a laforin-dependent manner, and targets it for proteasome-dependent degradation and this degradation decreases glycogen accumulation. Polyubiquitinates EPM2A/laforin and ubiquitinates AGL and targets them for proteasome-dependent degradation. Defects in NHLRC1 are a cause of progressive myoclonic epilepsy type 2 (EPM2); also known as Lafora disease. EPM2 is an autosomal recessive and severe form of adolescent-onset progressive epilepsy. Typically, as seizures increase in frequency, cognitive function declines towards dementia, and affected individuals die usually within 10 years after onset. EPM2 occurs worldwide, but it is particularly common in the mediterranean countries of southern Europe and northern Africa, in southern India and in the Middle East. At the cellular level, it is characterized by accumulation of starch-like polyglucosans called Lafora bodies (LBs) that are most abundant in organs with the highest glucose metabolism: brain, heart, liver and skeletal muscle. Among other conditions involving polyglucosans, EPM2 is unique in that the inclusions are in neuronal dendrites but not axons and the forming polyglucosan fibrils are associated with the endoplasmic reticulum.

Protein type: Ligase; Ubiquitin ligase; Ubiquitin conjugating system; EC 6.3.2.19; EC 6.3.2.-

Chromosomal Location of Human Ortholog: 6p22.3

Cellular Component: endoplasmic reticulum; perinuclear region of cytoplasm; cytosol; nucleus

Molecular Function: protein binding; zinc ion binding; ubiquitin-protein ligase activity; ligase activity

Biological Process: proteasomal ubiquitin-dependent protein catabolic process; glycogen biosynthetic process; protein polyubiquitination; positive regulation of protein ubiquitination; carbohydrate metabolic process; glucose metabolic process; autophagy; pathogenesis

Disease: Myoclonic Epilepsy Of Lafora

Research Articles on NHLRC1

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Product Notes

The Human NHLRC1 nhlrc1 (Catalog #AAA9329125) is an ELISA Kit and is intended for research purposes only. The product is available for immediate purchase. The AAA9329125 ELISA Kit recognizes Human NHLRC1. It is sometimes possible for the material contained within the vial of "NHL repeat containing 1, ELISA Kit" to become dispersed throughout the inside of the vial, particularly around the seal of said vial, during shipment and storage. We always suggest centrifuging these vials to consolidate all of the liquid away from the lid and to the bottom of the vial prior to opening. Please be advised that certain products may require dry ice for shipping and that, if this is the case, an additional dry ice fee may also be required.

Precautions

All products in the AAA Biotech catalog are strictly for research-use only, and are absolutely not suitable for use in any sort of medical, therapeutic, prophylactic, in-vivo, or diagnostic capacity. By purchasing a product from AAA Biotech, you are explicitly certifying that said products will be properly tested and used in line with industry standard. AAA Biotech and its authorized distribution partners reserve the right to refuse to fulfill any order if we have any indication that a purchaser may be intending to use a product outside of our accepted criteria.

Disclaimer

Though we do strive to guarantee the information represented in this datasheet, AAA Biotech cannot be held responsible for any oversights or imprecisions. AAA Biotech reserves the right to adjust any aspect of this datasheet at any time and without notice. It is the responsibility of the customer to inform AAA Biotech of any product performance issues observed or experienced within 30 days of receipt of said product. To see additional details on this or any of our other policies, please see our Terms & Conditions page.

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