WB result of NMNAT1 Recombinant Rabbit mAb
Primary antibody: NMNAT1 Recombinant Rabbit mAb at 1/1000 dilution
Lane 1: Caco-2 whole cell lysate 20 µg
Lane 2: MCF7 whole cell lysate 20 µg
Lane 3: 293T whole cell lysate 20 µg
Lane 4: HeLa whole cell lysate 20 µg
Lane 5: SK-MEL-28 whole cell lysate 20 µg
Low expression control: Caco-2 whole cell lysate
Secondary antibody: Goat Anti- rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 32 kDa
Observed MW: 30 kDa
Product Details
Product Details
Product Specification
| Host | Rabbit |
| Antigen | NMNAT1 |
| Synonyms | Nicotinamide/nicotinic acid mononucleotide adenylyltransferase 1; Nicotinamide-nucleotide adenylyltransferase 1 (NMN adenylyltransferase 1); Nicotinate-nucleotide adenylyltransferase 1 (NaMN adenylyltransferase 1); NMNAT |
| Immunogen | Synthetic Peptide |
| Location | Nucleus |
| Accession | Q9HAN9 |
| Clone Number | S-3703-4 |
| Antibody Type | Recombinant mAb |
| Isotype | IgG |
| Application | WB |
| Reactivity | Hu |
| Positive Sample | MCF7, 293T, HeLa, SK-MEL-28 |
| Purification | Protein A |
| Concentration | 0.5 mg/ml |
| Conjugation | Unconjugated |
| Physical Appearance | Liquid |
| Storage Buffer | PBS, 40% Glycerol, 0.05% BSA, 0.03% Proclin 300 |
| Stability & Storage | 12 months from date of receipt / reconstitution, -20 °C as supplied |
Dilution
| application | dilution | species |
| WB | 1:1000 | Hu |
Background
NMNAT1 (Nicotinamide Mononucleotide Adenylyltransferase 1) is a nuclear-localized enzyme that serves as the rate-limiting catalyst in the final step of the NAD+ salvage pathway, converting nicotinamide mononucleotide (NMN) and ATP into nicotinamide adenine dinucleotide (NAD+). As the primary isoform responsible for maintaining nuclear NAD+ pools, NMNAT1 is essential for supporting the activity of NAD+-dependent enzymes such as PARPs (poly-ADP-ribose polymerases) and sirtuins, which are critical for DNA repair, genomic stability, and epigenetic regulation. Beyond its metabolic function, NMNAT1 acts as a potent neuroprotective factor; it has been shown to delay Wallerian degeneration and protect axons from injury-induced degradation, a property largely attributed to its ability to sustain local NAD+ levels and stabilize cellular energy homeostasis. Mutations in the NMNAT1 gene are associated with Leber congenital amaurosis type 9 (LCA9), a severe early-onset retinal dystrophy, highlighting its indispensable role in neuronal and retinal health.
Picture
Picture
Western Blot
