Myosin 9 anticorps (N-Term)
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- Antigène Voir toutes Myosin 9 (MYH9) Anticorps
- Myosin 9 (MYH9)
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Épitope
- N-Term
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp Myosin 9 est non-conjugé
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Application
- Western Blotting (WB), Immunofluorescence (IF), Immunoprecipitation (IP), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC)
- Specificité
- This antibody may cross react with MYH10, MYH14, or other family members.
- Réactivité croisée
- Humain
- Attributs du produit
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Rabbit Polyclonal antibody to MYH9 (myosin, heavy chain 9, non-muscle)
MYH9 antibody [N1], N-term - Purification
- Purified by antigen-affinity chromatography.
- Classe de qualité
- KO Validated
- Immunogène
- Recombinant protein encompassing a sequence within the N-terminus region of human MYH9. The exact sequence is proprietary.
- Isotype
- IgG
- Top Product
- Discover our top product MYH9 Anticorps primaire
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- Indications d'application
- WB: 1:500-1:3000. IHC-P: 1:100-1:1000. IP: 1:100-1:500. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
- Commentaires
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Positive Control: U87-MG , SK-N-SH , IMR32 , SK-N-AS , NT2D1 , PC-3
Validation: KO/KD, Overexpression
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1.31 mg/mL
- Buffer
- 1XPBS pH 7, 20 % Glycerol, 0.025 % ProClin 300
- Agent conservateur
- ProClin
- Précaution d'utilisation
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Stock
- 4 °C,-20 °C
- Stockage commentaire
- Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
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- Antigène
- Myosin 9 (MYH9)
- Autre désignation
- myosin heavy chain 9 (MYH9 Produits)
- Sujet
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This gene encodes 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.
- Poids moléculaire
- 227 kDa
- ID gène
- 4627
- UniProt
- P35579
- Pathways
- Regulation of G-Protein Coupled Receptor Protein Signaling, Integrin Complex
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