BHMT2 Antikörper

Produktnummer ABIN7246028

Produktdetails anti-BHMT2 Antikörper

Target: BHMT2 (Betaine--Homocysteine S-Methyltransferase 2 (BHMT2))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser BHMT2 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA, Immunohistochemistry (IHC)

Produktmerkmale: Polyclonal Antibody

Aufreinigung: Antigen affinity purification

Immunogen: Fusion protein of human BHMT2

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:1000-1:5000, IHC 1:30-1:150, ELISA 1:5000-1:10000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.78 mg/mL

Buffer: PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

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 BHMT2

Target: BHMT2 (Betaine--Homocysteine S-Methyltransferase 2 (BHMT2))

Andere Bezeichnung: BHMT2 (BHMT2 Produkte)

Synonyme: C81077 antikoerper, D13Ucla2 antikoerper, BHMT2 antikoerper, DKFZp469M1332 antikoerper, bhmt-2 antikoerper, betaine--homocysteine S-methyltransferase 2 antikoerper, betaine-homocysteine methyltransferase 2 antikoerper, betaine-homocysteine S-methyltransferase 2 antikoerper, S-methylmethionine--homocysteine S-methyltransferase BHMT2 antikoerper, BHMT2 antikoerper, Bhmt2 antikoerper, LOC100073266 antikoerper

Hintergrund: Homocysteine is a sulfur-containing amino acid that plays a crucial role in methylation reactions. Transfer of the methyl group from betaine to homocysteine creates methionine, which donates the methyl group to methylate DNA, proteins, lipids, and other intracellular metabolites. The protein encoded by this gene is one of two methyl transferases that can catalyze the transfer of the methyl group from betaine to homocysteine. Anomalies in homocysteine metabolism have been implicated in disorders ranging from vascular disease to neural tube birth defects such as spina bifida. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

Molekulargewicht:

Observed_MW: Refer to figures

Calculated_MW: 40 kDa

UniProt: Q9H2M3

Pathways: Methionine Biosynthetic Process