SMCR7 anticorps (AA 201-300) (Cy3)

N° du produit ABIN6944934

Cet anticorps Lapin Polyclonal détecte spécifiquement SMCR7 dans IF (cc) et IF (p). Il présente une réactivité envers Souris.

Aperçu rapide pour SMCR7 anticorps (AA 201-300) (Cy3) (ABIN6944934)

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

Reactivité: Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SMCR7 est conjugé à/à la Cy3

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

Détail du produit anti-SMCR7 anticorps (Cy3)

Épitope: AA 201-300

Réactivité croisée: Souris

Homologie: Human,Dog,Cow,Sheep,Horse,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human SMCR7

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Stockage

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.

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur SMCR7

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

Autre désignation: SMCR7

Sujet:

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]

ID gène: 125170

UniProt: Q96C03