SMCR7 antibody (AA 201-300) (FITC)

Catalog No. ABIN6944938

The Rabbit Polyclonal anti-SMCR7 antibody is suitable to detect SMCR7 in samples from Mouse. It has been validated for IF (cc) and IF (p).

Quick Overview for SMCR7 antibody (AA 201-300) (FITC) (ABIN6944938)

Target: SMCR7 (Smith-Magenis Syndrome Chromosome Region, Candidate 7 (SMCR7))

Reactivity: Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SMCR7 antibody is conjugated to FITC

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

Product Details anti-SMCR7 Antibody (FITC)

Binding Specificity: AA 201-300

Cross-Reactivity: Mouse

Predicted Reactivity: Human,Dog,Cow,Sheep,Horse,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human SMCR7

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 SMCR7

Target: SMCR7 (Smith-Magenis Syndrome Chromosome Region, Candidate 7 (SMCR7))

Alternative Name: SMCR7

Background:

Synonyms: MGC23130, MID49, MIEF2, Mitochondrial dynamic protein MID49, Mitochondrial dynamic protein of 49 kDa, Mitochondrial elongation factor 2, Smith Magenis syndrome chromosome region candidate 7, Smith-Magenis syndrome chromosomal region candidate gene 7 protein.

Background: This gene encodes an outer mitochondrial membrane protein that functions in the regulation of mitochondrial morphology. It can directly recruit the fission mediator dynamin-related protein 1 (Drp1) to the mitochondrial surface. The gene is located within the Smith-Magenis syndrome region on chromosome 17. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jun 2011]

Gene ID: 125170

UniProt: Q96C03