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Receptor Accessory Protein 1 (REEP1) ELISA Kits

REEP1 encodes a mitochondrial protein that functions to enhance the cell surface expression of odorant receptors. Additionally we are shipping Receptor Accessory Protein 1 Antibodies (50) and Receptor Accessory Protein 1 Proteins (3) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
Anti-Human REEP1 REEP1 65055 Q9H902
Anti-Mouse REEP1 REEP1 52250 Q8BGH4
Anti-Rat REEP1 REEP1 362384  
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More ELISA Kits for Receptor Accessory Protein 1 Interaction Partners

Human Receptor Accessory Protein 1 (REEP1) interaction partners

  1. This study demonstrated that REEP1 gene mutation associated with hereditary spastic paraplegias in group of Polish patients

  2. we show that REEP1 facilitates endoplasmic reticulum mitochondria interactions, a function diminished by disease-associated mutations.

  3. Nonsense variants in REEP1 causing haploinsufficiency/loss of function are responsible for autosomal dominant hereditary spastic paraplegia (HSP)-type SPG31.

  4. Functional mutation analysis reveal that distinct pathomechanisms are associated with REEP1 mutations and shed new light on its probable functions.

  5. Expression of the REEP1/REEP2 (show REEP2 ELISA Kits) subfamily appears to be restricted to neuronal and neuronal-like exocytotic tissues, consistent with neuronally restricted symptoms of REEP1 genetic disorders.

  6. REEP1 is a neuron-specific, membrane-binding, and membrane curvature-inducing protein that resides in the endoplasmic reticulum.

  7. A novel REEP1 mutation is identified in a cohort of patients with upper motor neuron syndrome.

  8. Whole-exome sequencing of two affected individuals revealed a single candidate variant within the linking regions, i.e., a splice-site alteration in REEP1

  9. Identification of 12 different heterozygous REEP1 mutations, including two exon deletions, associated with either a pure or a complex phenotype.

  10. previously unreported autosomal dominant mutations in the REEP1 gene in hereditary spastic paraplegia

Mouse (Murine) Receptor Accessory Protein 1 (REEP1) interaction partners

  1. Functional mutation analysis reveal that distinct pathomechanisms are associated with REEP1 mutations and shed new light on its probable functions.

Receptor Accessory Protein 1 (REEP1) Antigen Profile

Antigen Summary

This gene encodes a mitochondrial protein that functions to enhance the cell surface expression of odorant receptors. Mutations in this gene cause spastic paraplegia autosomal dominant type 31, a neurodegenerative disorder. Alternative splicing results in multiple transcript variants.

Gene names and symbols associated with REEP1

  • receptor accessory protein 1 (REEP1) antibody
  • receptor accessory protein 1 (Reep1) antibody
  • C2orf23 antibody
  • D6Ertd253e antibody
  • HMN5B antibody
  • RGD1305230 antibody
  • SPG31 antibody

Protein level used designations for REEP1

receptor expression-enhancing protein 1 , receptor expression enhancing protein 1

GENE ID SPECIES
65055 Homo sapiens
52250 Mus musculus
362384 Rattus norvegicus
771776 Gallus gallus
613003 Canis lupus familiaris
616916 Bos taurus
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