MTR antibody (AA 1001-1100) (AbBy Fluor® 647)

Catalog No. ABIN6980090

The Rabbit Polyclonal anti-MTR antibody has been validated for WB, IF (cc) and IF (p). It is suitable to detect MTR in samples from Human and Rat.

Quick Overview for MTR antibody (AA 1001-1100) (AbBy Fluor® 647) (ABIN6980090)

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

Reactivity: Human, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This MTR antibody is conjugated to AbBy Fluor® 647

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

Product Details anti-MTR Antibody (AbBy Fluor® 647)

Binding Specificity: AA 1001-1100

Cross-Reactivity: Human, Rat

Predicted Reactivity: Mouse,Dog,Cow,Pig,Horse,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human MTR

Isotype: IgG

Application Details

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

Restrictions: For Research Use only

Handling

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.

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for MTR

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

Alternative Name: MTR

Background:

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.

Gene ID: 238505

UniProt: Q99707

Pathways: Methionine Biosynthetic Process