SMCR7 anticorps (AA 201-300) (Biotin)

N° du produit ABIN6944926

L’anticorps Lapin Polyclonal anti-SMCR7 a été validé pour ELISA, IHC (fro) et IHC (p). Il convient pour détecter SMCR7 dans des échantillons de Souris.

Aperçu rapide pour SMCR7 anticorps (AA 201-300) (Biotin) (ABIN6944926)

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 Biotin

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

Détail du produit anti-SMCR7 anticorps (Biotin)

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

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 for 12 months.

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