Myosin VIIA anticorps (AA 830-910)
Aperçu rapide pour Myosin VIIA anticorps (AA 830-910) (ABIN7229866)
Antigène
Voir toutes Myosin VIIA (MYO7A) AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- AA 830-910
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Fonction
- MYO7A Polyclonal Antibody
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Specificité
- The antibody detects endogenous levels of MYO7A protein
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Purification
- The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen
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Immunogène
- Synthesized peptide derived from part region of human MYO7A protein at AA range: 830-910
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Isotype
- IgG
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Indications d'application
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).
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Commentaires
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Primary Antibody
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 mg/mL
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Buffer
- PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.
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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
- -20 °C
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Stockage commentaire
- Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
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- Myosin VIIA (MYO7A)
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Autre désignation
- MYO7A
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Sujet
- Rabbit Anti-MYO7A Polyclonal Antibody,Unconventional myosin-VIIa,MYO7A (Myosin VIIA) is a Protein Coding gene. Among its related pathways are Sertoli-Sertoli Cell Junction Dynamics and Actin Nucleation by ARP-WASP Complex. MYO7A is a member of the myosin gene family. Myosins are mechanochemical proteins characterized by the presence of a motor domain, an actin-binding domain, a neck domain that interacts with other proteins, and a tail domain that serves as an anchor. MYO7A encodes an unconventional myosin with a very short tail. Defects in MYO7A are associated with the mouse shaker-1 phenotype and the human Usher syndrome 1B which are characterized by deafness, reduced vestibular function, and (in human) retinal degeneration. Alternative splicing results in multiple transcript variants.,MYO7A
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Poids moléculaire
- observerd band 243kDa
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ID gène
- 4647
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UniProt
- Q13402
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Pathways
- Sensory Perception of Sound
Antigène
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