MTR anticorps (AA 1001-1100) (Biotin)

N° du produit ABIN5675444

Cet anticorps anti-MTR Polyclonal Lapin conjugué à Biotin (ABIN5675444) détecte spécifiquement MTR dans WB, ELISA, IHC (p) et IHC (fro). L’anticorps est réactif avec des échantillons de Humain et Rat.

Aperçu rapide pour MTR anticorps (AA 1001-1100) (Biotin) (ABIN5675444)

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

Reactivité: Humain, Rat

Hôte: Lapin

Clonalité: Polyclonal

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

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

Détail du produit anti-MTR anticorps (Biotin)

Épitope: AA 1001-1100

Réactivité croisée: Humain, Rat

Homologie: Mouse,Dog,Cow,Pig,Horse,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human MTR

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 MTR

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

Autre désignation: MTR

Sujet:

Synonyms: Methionine synthase, MTR, 5-methyltetrahydrofolate--homocysteine, methyltransferase, Vitamin-B12 dependent methionine synthase, MS

Background: MTR encodes the enzyme 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.

ID gène: 238505

UniProt: Q99707

Pathways: Methionine Biosynthetic Process