Myosin 9 anticorps (Middle Region)
Aperçu rapide pour Myosin 9 anticorps (Middle Region) (ABIN2783216)
Antigène
Voir toutes Myosin 9 (MYH9) AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- Middle Region
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Fonction
- MYH9 Antibody - middle region
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Séquence
- DAMNREVSSL KNKLRRGDLP FVVPRRMARK GAGDGSDEEV DGKADGAEAK
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Homologie
- Dog: 93%, Guinea Pig: 86%, Human: 100%, Mouse: 86%, Pig: 93%, Rabbit: 86%, Rat: 93%
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Attributs du produit
- This is a rabbit polyclonal antibody against MYH9. It was validated on Western Blot using a cell lysate as a positive control.
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Purification
- Affinity Purified
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Immunogène
- The immunogen is a synthetic peptide directed towards the middle region of human MYH9
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Indications d'application
- Optimal working dilution should be determined by the investigator.
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Commentaires
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We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP48072-100UG
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 0.5 mg/mL
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Buffer
- Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
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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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Conseil sur la manipulation
- prevent freeze-thaw cycles
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Stock
- 4 °C,-20 °C
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Stockage commentaire
- For short term use, store at 2-8C up to 1 week. For long term storage, store at -20 °C in small aliquots to prevent freeze-thaw cycles.
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: "Dlc1 interaction with non-muscle myosin heavy chain II-A (Myh9) and Rac1 activation." dans: Biology open, Vol. 5, Issue 4, pp. 452-60, (2016) (PubMed).
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- Myosin 9 (MYH9)
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Autre désignation
- MYH9
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Sujet
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Background Information: MYH9 is a myosin IIA heavy chain that contains an IQ domain and a myosin head-like domain. The protein is involved in several important functions, including cytokinesis, cell motility and maintenance of cell shape. Defects in MYH9 are the cause of non-syndromic sensorineural deafness autosomal dominant type 17, Epstein syndrome, Alport syndrome with macrothrombocytopenia, Sebastian syndrome, Fechtner syndrome and macrothrombocytopenia with progressive sensorineural deafness.
Gene Name: Myosin, heavy chain 9, non-muscle
Alternative Symbols: MHA, FTNS, EPSTS, BDPLT6, DFNA17, MATINS, NMMHCA, NMHC-II-A, NMMHC-IIA
Protein Name: Myosin-9
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Poids moléculaire
- 226kDa
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ID gène
- 4627
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NCBI Accession
- NP_002464
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UniProt
- P35579
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Pathways
- Regulation of G-Protein Coupled Receptor Protein Signaling, Integrin Complex
Antigène
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