N-Alpha-Acetyltransferase 10 (NAA10) Antibody

Por favor contáctenos para obtener información detallada sobre el precio y disponibilidad.
Description
NAA10 Antibody is a Rabbit Polyclonal antibody against NAA10. N-alpha-acetylation is among the most common post-translational protein modifications in eukaryotic cells. This process involves the transfer of an acetyl group from acetyl-coenzyme A to the alpha-amino group on a nascent polypeptide and is essential for normal cell function. This gene encodes an N-terminal acetyltransferase that functions as the catalytic subunit of the major amino-terminal acetyltransferase A complex. Mutations in this gene are the cause of Ogden syndrome. Alternate splicing results in multiple transcript variants.
Documents del producto
Product specifications
Category | Primary Antibodies |
Immunogen Target | N-Alpha-Acetyltransferase 10 (NAA10) |
Host | Rabbit |
Reactivity | Human, Mouse, Rat |
Recommended Dilution | ELISA: 1 µg/ml, WB: 1/500 - 1/2000, IHC-P: 1/50 - 1/200, IF/ICC: 1/50 - 1/100. Not tested in IHC-F. Optimal dilutions/concentrations should be determined by the end user. |
Clonality | Polyclonal |
Conjugation | Unconjugated |
Isotype | IgG |
Purification | Purified by affinity chromatography. |
Size 1 | 20 µl |
Size 2 | 100 µl |
Size 3 | 2 × 100 µl |
Form | Liquid |
Tested Applications | ELISA, WB, IHC, IF/ICC |
Buffer | PBS, pH 7.3, containing 0.02% sodium azide, 50% glycerol. |
Availability | Shipped within 5-10 working days. |
Storage | Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles. |
Dry Ice | No |
UniProt ID | P41227 |
Gene ID | 8260 |
NCBI Accession | NP_003482.1 |
Background | Antibody anti-NAA10 |
Status | RUO |
Note | Concentration: > 0.2 mg/ml - |
Descripción
Related Products

Recombinant Human NAA10
Ver Producto
N-Alpha-Acetyltransferase 10 (NAA10) Antibody
NAA10 Antibody is a Rabbit Polyclonal antibody against NAA10. N-alpha-acetylation is among the most common post-translational protein modifications in eukaryotic cells. This process involves the transfer of an acetyl group from acetyl-coenzyme A to the alpha-amino group on a nascent polypeptide and is essential for normal cell function. This gene encodes an N-terminal acetyltransferase that functions as the catalytic subunit of the major amino-terminal acetyltransferase A complex. Mutations in this gene are the cause of Ogden syndrome. Alternate splicing results in multiple transcript variants.
Ver Producto
Human N-Alpha-Acetyltransferase 10 (NAA10) Protein
N Alpha-Acetyltransferase 10, NatA Catalytic Subunit is a recombinant enzyme.
Ver Producto