NAA10 Antikörper (AA 161-235)

Produktnummer ABIN6144318

Produktdetails anti-NAA10 Antikörper

Target: NAA10 (ARD1A) (ARD1 Homolog, N-Acetyltransferase (ARD1A))

Bindungsspezifität: AA 161-235

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser NAA10 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)

Sequenz: HLELKEKGRH VVLGAIENKV ESKGNSPPSS GEACREEKGL AAEDSGGDSK DLSEVSETTE STDVKDSSEA SDSAS

Kreuzreaktivität: Human, Maus, Ratte

Produktmerkmale: Polyclonal Antibodies

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 161-235 of human NAA10 (NP_003482.1).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB,1:500 - 1:2000,IHC,1:50 - 1:200,IF,1:50 - 1:100

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu NAA10

Target: NAA10 (ARD1A) (ARD1 Homolog, N-Acetyltransferase (ARD1A))

Andere Bezeichnung: NAA10 (ARD1A Produkte)

Synonyme: ARD1 antikoerper, ARD1A antikoerper, DXS707 antikoerper, NATD antikoerper, TE2 antikoerper, 2310039H09Rik antikoerper, Ard1 antikoerper, Ard1a antikoerper, Te2 antikoerper, RGD1565315 antikoerper, N(alpha)-acetyltransferase 10, NatA catalytic subunit antikoerper, NAA10 antikoerper, Naa10 antikoerper

Hintergrund: 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.,NAA10,ARD1,ARD1A,ARD1P,DXS707,MCOPS1,NATD,OGDNS,TE2,Epigenetics & Nuclear Signaling,Signal Transduction,Endocrine & Metabolism,Amino acid metabolism,NAA10

Molekulargewicht: 24 kDa/26 kDa

Gen-ID: 8260

UniProt: P41227