MTR anticorps (AA 1001-1100) (Alexa Fluor 555)

N° du produit ABIN6978436

Détail du produit anti-MTR anticorps (Alexa Fluor 555)

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

Épitope: AA 1001-1100

Reactivité: Humain, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MTR est conjugé à/à la Alexa Fluor 555

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

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: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur MTR

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

Autre désignation: MTR (MTR Produits)

Synonymes: anticorps HMAG, anticorps MS, anticorps cblG, anticorps AI894170, anticorps D830038K18Rik, anticorps methioninesynthase, anticorps 5-methyltetrahydrofolate-homocysteine methyltransferase, anticorps MTR, anticorps 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