Nicotinamide Nucleotide Adenylyltransferase 1 (NMNAT1) ELISA Kits

NMNAT1 encodes an enzyme which catalyzes a key step in the biosynthesis of the coenzyme NAD. Additionally we are shipping NMNAT1 Antibodies (88) and NMNAT1 Proteins (18) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
NMNAT1 64802 Q9HAN9
NMNAT1 66454 Q9EPA7
Anti-Rat NMNAT1 NMNAT1 298653  
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Top NMNAT1 ELISA Kits at

Showing 3 out of 8 products:

Catalog No. Reactivity Sensitivity Range Images Quantity Supplier Delivery Price Details
Mouse 9.375 pg/mL 15.6 pg/mL - 1000 pg/mL A typical standard curve 96 Tests Log in to see 13 to 16 Days
Human 0.8 pg/mL n/a   96 Tests Log in to see 11 to 16 Days
  96 Tests Log in to see 15 to 18 Days

More ELISA Kits for NMNAT1 Interaction Partners

Human Nicotinamide Nucleotide Adenylyltransferase 1 (NMNAT1) interaction partners

  1. Results associate a distinct retinal dystrophy phenotype with nicotinamide-nucleotide adenylyltransferase 1 protein (NMNAT1) mutation and suggest coiled-coil domain containing 66 (CCDC66) should not be considered a retinal dystrophy candidate gene.

  2. Hidden Genetic Variation in LCA9-Associated Congenital Blindness Explained by 5'UTR (show UTS2R ELISA Kits) Mutations and Copy-Number Variations of NMNAT1.

  3. We confirmed a diagnosis of NMNAT1-associated Leber congenital amaurosis in two siblings through identification of the mutation (c.25G>A [p. Val9Met]) in a homozygous state.

  4. NMNAT1, which encodes the nicotinamide mononucleotide adenylyltransferase 1, has been recently identified to be one of the LCA-causing genes. Our results expanded the spectrum of mutations in NMNAT1

  5. To study how mutations affect NMNAT1 function and ultimately lead to a retinal degeneration phenotype, we performed detailed analysis of Leber congenital amaurosis 9-associated NMNAT1 mutants.

  6. theNMNAT1 p.Glu257Lys variant is a hypomorphic variant that almost without exception causes leber congenital amaurosis (LCA) in combination with more severe NMNAT1 variants.

  7. The aim of this study was to determine the occurrence and frequency of NMNAT1 mutations and associated phenotypes in different types of inherited retinal dystrophies.

  8. Data found pathogenic DNA variants in the genes RP1, USH2A, CNGB3, NMNAT1, CHM, and ABCA4, responsible for retinitis pigmentosa, Usher syndrome, achromatopsia, Leber congenital amaurosis, choroideremia, or recessive Stargardt/cone-rod dystrophy cases.

  9. NMNAT1 deletion in tumors may contribute to transformation by increasing ribosomal RNA synthesis.

  10. mutations in nicotinamide nucleotide adenylyltransferase 1(NMNAT1) cause Leber congenital amaurosis

Mouse (Murine) Nicotinamide Nucleotide Adenylyltransferase 1 (NMNAT1) interaction partners

  1. that increasing NMNAT1 levels can slow the progression of symptoms and neuropathological features of tauopathy

  2. Using steady-state and flux analysis of NAD(+) metabolites in healthy and injured mouse dorsal root ganglion axons, we find that rather than altering NAD(+) synthesis, NMNAT1 instead blocks the injury-induced, SARM1-dependent NAD(+) consumption that is central to axon degeneration.

  3. NMNAT1 overexpression enhanced AMPK (show PRKAA1 ELISA Kits) activity in oxygen-glucose deprivation treated cortical neurons

  4. An increased level of Nmnat protein in hiw mutants is both required and sufficient to inhibit axonal degeneration.

  5. Overexpression of Nmnat1 in the cytoplasm and axons of RGCs robustly protected against both ischemic and glaucomatous loss of RGC axonal integrity, as well as loss of RGC soma.

  6. Findings reveal a novel role for NMNAT1 in the morphogenesis of developing cortical neurons, which indicate that the loss of function of NMNAT1 may contribute to different neurodegenerative disorders in central nervous system.

  7. Nicotinamide mononucleotide adenylyl transferase 1 protects against acute neurodegeneration in developing CNS by inhibiting excitotoxic-necrotic cell death.

  8. NMNAT1 is indispensable for the normal development of the embryo. Decreased NMNAT1 activity in heterozygous null mice does not affect the rate of Wallerian degeneration, suggesting that endogenous NMNAT1 does not have a primary role in axon maintenance.

  9. nicotinamide mononucleotide adenylyltransferase (Nmnat) protein transduction into transected axons blocks axonal degeneration

  10. Through NAMPT (show NAMPT ELISA Kits) activity, visfatin (show NAMPT ELISA Kits) contributes to vascular inflammation, causing atherothrombotic diseases linked to metabolic disorders.

NMNAT1 Antigen Profile

Antigen Summary

This gene encodes an enzyme which catalyzes a key step in the biosynthesis of the coenzyme NAD. The encoded protein is one of several nicotinamide nucleotide adenylyltransferases. Studies in Drosophila and mammalian neurons have shown the encoded protein can confer protection to damaged neurons. This protection requires enzymatic activity which increases NAD levels and activates a nuclear deacetylase which is the protective molecule. Pseudogenes of this gene are located on chromosomes 1, 3, 4, 14 and 15.

Gene names and symbols associated with NMNAT1

  • nicotinamide mononucleotide adenylyltransferase 1 (CpipJ_CPIJ015320) antibody
  • nicotinamide mononucleotide adenylyltransferase 1 (PTRG_06486) antibody
  • nicotinamide nucleotide adenylyltransferase 1 (nmnat1) antibody
  • nicotinamide nucleotide adenylyltransferase 1 (NMNAT1) antibody
  • nicotinamide nucleotide adenylyltransferase 1 (Nmnat1) antibody
  • 2610529L11Rik antibody
  • 5730441G13Rik antibody
  • D4Cole1e antibody
  • id:ibd5068 antibody
  • im:7144541 antibody
  • LCA9 antibody
  • nmnat antibody
  • PNAT1 antibody
  • zgc:110243 antibody

Protein level used designations for NMNAT1

nicotinamide mononucleotide adenylyltransferase 1 , Nicotinamide mononucleotide adenylyltransferase 1 , NMN adenylyltransferase 1 , NaMN adenylyltransferase 1 , nicotinate-nucleotide adenylyltransferase 1 , pyridine nucleotide adenylyltransferase 1 , naMN adenylyltransferase 1 , NAD(+) diphosphorylase , NAD(+) pyrophosphorylase , deamido-NAD(+) diphosphorylase , deamido-NAD(+) pyrophosphorylase , nicotinamide mononucleotide adenylyl transferase , nicotinamide/nicotinate mononucleotide adenylyltransferase 1 , nicotinamide mononucleotide adenylyl transferase 1

6048336 Culex quinquefasciatus
6344745 Pyrenophora tritici-repentis Pt-1C-BFP
100194756 Salmo salar
550322 Danio rerio
419446 Gallus gallus
64802 Homo sapiens
479601 Canis lupus familiaris
522863 Bos taurus
66454 Mus musculus
298653 Rattus norvegicus
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