N6AMT1 anticorps (AA 1-100) (Biotin)

N° du produit ABIN1700337

Cet anticorps anti-N6AMT1 est un anticorps Lapin Polyclonal détectant N6AMT1 dans WB, ELISA, IHC (fro) et IHC (p). Adapté pour Humain.

Aperçu rapide pour N6AMT1 anticorps (AA 1-100) (Biotin) (ABIN1700337)

Antigène: N6AMT1 (N-6 Adenine-Specific DNA Methyltransferase 1 (Putative) (N6AMT1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp N6AMT1 est conjugé à/à la Biotin

Application: Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-N6AMT1 anticorps (Biotin)

Épitope: AA 1-100

Réactivité croisée: Humain

Homologie: Mouse,Rat,Sheep,Horse

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human HEMK2

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C for 12 months.

Date de péremption: 12 months

Détails sur N6AMT1

Antigène: N6AMT1 (N-6 Adenine-Specific DNA Methyltransferase 1 (Putative) (N6AMT1))

Autre désignation: HEMK2

Sujet:

Synonyms: C21orf127, Chromosome 21 open reading frame 127, EC 2.1.1.-, HemK methyltransferase family member 2, HemK2, M.HsaHemK2P, MGC19995, MTQ2, N-6 adenine-specic DNA methyltransferase 1, N-6 adenine-specic DNA methyltransferase 1 putative, N6-DNA-methyltransferase, N6AMT, N6AMT1, OTTHUMP00000096393, OTTHUMP00000096394, PRED28, HEMK2_HUMAN.

Background: HEMK2 is a 214 amino acid protein that belongs to the methyltransferase superfamily and exists as multiple alternatively spliced isoforms. The gene encoding HEMK2 maps to human chromosome 21, which houses approximately 300 genes and comprises nearly 1.5 % of the human genome. Chromosome 21-associated disorders include Alzheimer's disease, amyotrophic lateral sclerosis and, most notably, Down syndrome (also known as trisomy 21).

ID gène: 29104