MECR antibody (AA 39-359)

Catalog No. ABIN8010772

The Rabbit Polyclonal anti-MECR antibody (ABIN8010772) specifically detects MECR in WB, ELISA, IHC and FACS. The antibody is reactive with Human, Mouse and Rat samples.

Quick Overview for MECR antibody (AA 39-359) (ABIN8010772)

Target: MECR (Mitochondrial Trans-2-Enoyl-CoA Reductase (MECR))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This MECR antibody is un-conjugated

Application: Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Flow Cytometry (FACS)

Grade: Carrier-free

Product Details anti-MECR Antibody

Binding Specificity: AA 39-359

Purpose: Anti-MECR Antibody

Cross-Reactivity (Details): No cross-reactivity with other proteins.

Characteristics: Anti-MECR Antibody. Tested in ELISA, IHC, WB, Flow Cytometry applications. This antibody reacts with Human, Mouse, Rat.

Purification: Immunogen affinity purified.

Immunogen: E.coli-derived human MECR recombinant protein (Position: E39-A359).

Isotype: IgG

Application Details

Application Notes: Western blot, 0.25-0.5 μg/mL, Human, Mouse, Rat Immunohistochemistry(Paraffin-embedded Section), 1-2 μg/mL, Human Flow Cytometry (Fixed), 1-3 μg/1x10⁶ cells, Human ELISA, 0.1-0.5 μg/mL, -

Restrictions: For Research Use only

Handling

Format: Lyophilized

Reconstitution: Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

Concentration: 500 μg/mL

Buffer: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

Storage: 4 °C,-20 °C

Storage Comment: At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.

Expiry Date: 12 months

Target Details for MECR

Target: MECR (Mitochondrial Trans-2-Enoyl-CoA Reductase (MECR))

Alternative Name: MECR

Background:

Background: Trans-2-enoyl-CoA reductase, mitochondrial is an enzyme that in humans is encoded by the MECR gene. The protein encoded by this gene is an oxidoreductase that catalyzes the last step in mitochondrial fatty acid synthesis. Defects in this gene are a cause of childhood-onset dystonia and optic atrophy.

Gene Full Name: mitochondrial trans-2-enoyl-CoA reductase

Molecular Weight: 38 kDa

Gene ID: 51102

UniProt: Q9BV79