MFN2 anticorps (AA 447-476)
Aperçu rapide pour MFN2 anticorps (AA 447-476) (ABIN652786)
Antigène
Voir toutes MFN2 AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
Clone
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Épitope
- AA 447-476
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Homologie
- Rat
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Purification
- This antibody is purified through a protein A column, followed by peptide affinity purification.
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Immunogène
- This MFN2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 447-476 amino acids from the Central region of human MFN2.
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Isotype
- Ig Fraction
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Indications d'application
- WB: 1:1000. IHC-P: 1:25. FC: 1:10~50
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Restrictions
- For Research Use only
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Format
- Liquid
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Buffer
- Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
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Agent conservateur
- Sodium azide
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Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Stock
- 4 °C,-20 °C
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Stockage commentaire
- Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.
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Date de péremption
- 6 months
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: "Downregulation of mitochondrial cyclooxygenase-2 inhibits the stemness of nasopharyngeal carcinoma by decreasing the activity of dynamin-related protein 1." dans: Theranostics, Vol. 7, Issue 5, pp. 1389-1406, (2018) (PubMed).
: "Evaluation of pancreatic cancer cell migration with multiple parameters in vitro by using an optical real-time cell mobility assay device." dans: BMC cancer, Vol. 17, Issue 1, pp. 234, (2017) (PubMed).
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: "Downregulation of mitochondrial cyclooxygenase-2 inhibits the stemness of nasopharyngeal carcinoma by decreasing the activity of dynamin-related protein 1." dans: Theranostics, Vol. 7, Issue 5, pp. 1389-1406, (2018) (PubMed).
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- MFN2 (Mitofusin 2 (MFN2))
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Autre désignation
- MFN2
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Sujet
- MFN2 is a mitochondrial membrane protein that participates in mitochondrial fusion and contributes to the maintenance and operation of the mitochondrial network. This protein is involved in the regulation of vascular smooth muscle cell proliferation, and it may play a role in the pathophysiology of obesity. Mutations in this gene cause Charcot-Marie-Tooth disease type 2A2, and hereditary motor and sensory neuropathy VI, which are both disorders of the peripheral nervous system.
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Poids moléculaire
- 86402
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ID gène
- 9927
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NCBI Accession
- NP_001121132, NP_055689
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UniProt
- O95140
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Pathways
- Skeletal Muscle Fiber Development
Antigène
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