Methylenetetrahydrofolate Reductase (MTHFR) Antibody

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195€ (20 µl)

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935106861
info@markelab.com
name
Methylenetetrahydrofolate Reductase (MTHFR) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx000043
tested applications
ELISA, WB

Description

MTHFR Antibody is a Mouse Polyclonal antibody against MTHFR. The protein encoded by this gene catalyzes the conversion of 5,10-methylenetetrahydrofolate to 5-methyltetrahydrofolate, a co-substrate for homocysteine remethylation to methionine. Genetic variation in this gene influences susceptibility to occlusive vascular disease, neural tube defects, colon cancer and acute leukemia, and mutations in this gene are associated with methylenetetrahydrofolate reductase deficiency.

Documents del producto

Instrucciones
Data sheet
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Product specifications

Category
Primary Antibodies
Immunogen Target
Methylenetetrahydrofolate Reductase (MTHFR)
Host
Rabbit
Reactivity
Rat
Recommended Dilution
ELISA: 1 µg/ml, WB: 1/500 - 1/2000. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Purification
Purified by affinity chromatography.
Size 1
20 µl
Size 2
100 µl
Size 3
2 × 100 µl
Form
Liquid
Tested Applications
ELISA, WB
Buffer
PBS, pH 7.3, containing 0.05% Proclin-300, 50% glycerol.
Availability
Shipped within 5-10 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
Q6P5Z2
Gene ID
4524
NCBI Accession
NP_005948.3
Background
Antibody anti-MTHFR
Status
RUO
Note
Concentration: > 0.2 mg/ml -

Descripción

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abx000043

Methylenetetrahydrofolate Reductase (MTHFR) Antibody

MTHFR Antibody is a Mouse Polyclonal antibody against MTHFR. The protein encoded by this gene catalyzes the conversion of 5,10-methylenetetrahydrofolate to 5-methyltetrahydrofolate, a co-substrate for homocysteine remethylation to methionine. Genetic variation in this gene influences susceptibility to occlusive vascular disease, neural tube defects, colon cancer and acute leukemia, and mutations in this gene are associated with methylenetetrahydrofolate reductase deficiency.

Ver Producto