MTR anticorps (AA 880-1095) (HRP)

N° du produit ABIN7965105

Cet anticorps anti-MTR Polyclonal Lapin conjugué à HRP (ABIN7965105) détecte spécifiquement MTR dans WB, ELISA et IHC. L’anticorps est réactif avec des échantillons de Humain, Rat et Souris.

Aperçu rapide pour MTR anticorps (AA 880-1095) (HRP) (ABIN7965105)

Antigène: MTR (5-Methyltetrahydrofolate-Homocysteine Methyltransferase (MTR))

Reactivité: Humain, Rat, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MTR est conjugé à/à la HRP

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

Détail du produit anti-MTR anticorps (HRP)

Épitope: AA 880-1095

Fonction: Anti-MTR Antibody HRP Conjugated

Specificité: No cross reactivity with other proteins.

Réactivité croisée (Details): No cross-reactivity with other proteins.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human MTR recombinant protein (Position: V880-D1095).

Isotype: IgG

Information d'application

Indications d'application: Western blot, Optimal dilutions should be determined by end users. Immunohistochemistry (Paraffin-embedded Section), Optimal dilutions should be determined by end users. ELISA, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4.

Stock: -20 °C

Stockage commentaire: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing.

Date de péremption: 12 months

Détails sur MTR

Antigène: MTR (5-Methyltetrahydrofolate-Homocysteine Methyltransferase (MTR))

Autre désignation: MTR

Sujet:

Background: Methionine synthase also known as MS, MeSe, MetH is responsible for the regeneration of methionine from homocysteine. In humans it is encoded by the MTR gene (5-methyltetrahydrofolate-homocysteine methyltransferase). It is mapped to 1q43. This gene encodes the 5-methyltetrahydrofolate-homocysteine methyltransferase. This enzyme, also known as cobalamin-dependent methionine synthase, catalyzes the final step in methionine biosynthesis. Mutations in MTR have been identified as the underlying cause of methylcobalamin deficiency complementation group G. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene.

Gene Full Name: 5-methyltetrahydrofolate-homocysteine methyltransferase

ID gène: 4548

UniProt: Q99707

Pathways: Methionine Biosynthetic Process