MTR antibody (AA 1001-1100) (Alexa Fluor 350)

Catalog No. ABIN6976714

Product Details anti-MTR Antibody (Alexa Fluor 350)

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

Binding Specificity: AA 1001-1100

Reactivity: Human, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This MTR antibody is conjugated to Alexa Fluor 350

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

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 (MTR Products)

Synonyms: HMAG antibody, MS antibody, cblG antibody, AI894170 antibody, D830038K18Rik antibody, methioninesynthase antibody, 5-methyltetrahydrofolate-homocysteine methyltransferase antibody, MTR antibody, Mtr antibody

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