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Invitrogen™ NHLRC1 Polyclonal Antibody
GREENER_CHOICE

Rabbit Polyclonal Antibody

Brand:  Invitrogen™ PA5121441

Product Code. 17792834

  • £438.00 / 100µL

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Description

Description

Antibody tested in Indirect ELISA.

Progressive myoclonic epilepsy type 2 (EPM2), also called Lafora disease, is an autosomal recessive disease characterized by grand mal seizures and/or myoclonus at about 15 years of age. Rapid and severe mental deterioration follows, often with psychotic features. Survival is less than 10 years after onset. Starch-like, endoplasmic reticulum-associated polyglucosans, called Lafora bodies, can be observed in brain, muscle, liver and heart. One cause of Lafora disease is due to mutations in NHLRC1, the gene encoding Malin. Forty-nine different mutations in NHLRC1 have been shown to cause EPM2. Malin, also called NHL repeat-containing protein 1, is a single subunit E3 ubiquitin ligase, containing 6 NHL repeats and 1 RING-type zinc finger. Malin's RING domain is responsible for its ability to mediate ubiquitination. Malin interacts with and polyubiquitinates Laforin, a protein also implicated in EPM2. Malin localizes to the endoplasmic reticulum and, to a lesser extent, in the nucleus. Malin is expressed in brain, cerebellum, spinal cord, medulla, heart, liver, skeletal muscle and pancreas.
TRUSTED_SUSTAINABILITY
Specifications

Specifications

NHLRC1
Polyclonal
Unconjugated
NHLRC1
AI505271; B230309E09Rik; bA204B7.2; E3 ubiquitin-protein ligase NHLRC1; EPM2A; EPM2B; Malin; NHL repeat containing 1; NHL repeat containing E3 ubiquitin protein ligase 1; NHL repeat-containing protein 1; NHLRC1; RING-type E3 ubiquitin transferase NHLRC1
Rabbit
Protein G
RUO
378884
-20°C or -80°C if preferred
Liquid
ELISA, Immunohistochemistry (Paraffin)
3.63 mg/mL
PBS with 50% glycerol and 0.03% ProClin 300; pH 7.4
Q6VVB1
NHLRC1
Recombinant Human E3 ubiquitin-protein ligase NHLRC1 protein (86-395aa).
100 μL
Primary
Human
Antibody
IgG
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