SMCR7 antibody (AA 201-300) (Biotin)

Catalog No. ABIN6944926

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

Quick Overview for SMCR7 antibody (AA 201-300) (Biotin) (ABIN6944926)

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

Reactivity: Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SMCR7 antibody is conjugated to Biotin

Application: ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Product Details anti-SMCR7 Antibody (Biotin)

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: IHC-P 1:200-400
IHC-F 1:100-500

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 for 12 months.

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