NAA10 Antikörper (AA 111-235)
-
- Target Alle NAA10 (ARD1A) Antikörper anzeigen
- NAA10 (ARD1A) (ARD1 Homolog, N-Acetyltransferase (ARD1A))
-
Bindungsspezifität
- AA 111-235
-
Reaktivität
- Human, Maus, Affe
-
Wirt
- Maus
-
Klonalität
- Monoklonal
-
Konjugat
- Dieser NAA10 Antikörper ist unkonjugiert
- Applikation
- Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Flow Cytometry (FACS), Immunocytochemistry (ICC), Neutralization (Neut)
- Aufreinigung
- purified
- Immunogen
- Purified recombinant fragment of human NAA10 (AA: 111-235) expressed in E. coli.
- Klon
- 3G3E9
- Isotyp
- IgG1
- Top Product
- Discover our top product ARD1A Primärantikörper
-
-
- Applikationshinweise
- ELISA: 1:10000, WB: 1:500 - 1:2000, ICC: 1:200 - 1:1000, FCM: N/A, IHC: N/A
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
-
- Format
- Liquid
- Buffer
- Purified antibody in PBS with 0.05 % sodium azide
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Lagerung
- 4 °C/-20 °C
- Informationen zur Lagerung
- 4°C, -20°C for long term storage
-
- 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
-
Description: 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.
Aliases: TE2, ARD1, NATD, ARD1A, ARD1P, OGDNS, DXS707, MCOPS1
- Molekulargewicht
- 26.5 kDa
- Gen-ID
- 8260
- HGNC
- 8260
-