Myosin VIIA anticorps

N° du produit ABIN2433419

Détail du produit anti-Myosin VIIA anticorps

Antigène: Myosin VIIA (MYO7A)

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Myosin VIIA est non-conjugé

Application: ELISA, Immunohistochemistry (IHC)

Purification: Affinity purification

Immunogène: Synthetic peptide of human MYO7A

Isotype: IgG

Information d'application

Indications d'application: IHC 1:50-1:200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.6 mg/mL

Buffer: PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

Agent conservateur: Sodium azide

Conseil sur la manipulation: Avoid freeze / thaw cycles.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur Myosin VIIA

Antigène: Myosin VIIA (MYO7A)

Autre désignation: MYO7A (MYO7A Produits)

Synonymes: anticorps 53D10S, anticorps BG:DS00929.11, anticorps CG7595, anticorps D, anticorps D2, anticorps DM7a, anticorps DMyoVIIa, anticorps Dm 35B, anticorps DmVIIA, anticorps DmVIIa, anticorps Dmel\\CG7595, anticorps Dro35B, anticorps ESTS:53D10S, anticorps Mhc35BC, anticorps MyoVIIA, anticorps anon-35Bb, anticorps br27, anticorps ck/MyoVIIA, anticorps l(1)35Ca, anticorps l(2)07130, anticorps l(2)35Ca, anticorps l(2)br27, anticorps l35Ca, anticorps myoVIIA, anticorps stc, anticorps stch, anticorps myo7a, anticorps MYO7A, anticorps NV17859, anticorps Hdb, anticorps Myo7, anticorps USH1B, anticorps nmf371, anticorps polka, anticorps sh-1, anticorps sh1, anticorps DFNA11, anticorps DFNB2, anticorps MYOVIIA, anticorps MYU7A, anticorps NSRD2, anticorps crinkled, anticorps myosin VIIAa, anticorps myosin VIIa, anticorps myosin VIIA, anticorps myosin 7A, anticorps myosin-VIIa, anticorps ck, anticorps myo7aa, anticorps LOAG_02192, anticorps MYO7A, anticorps myo7a, anticorps LOC663995, anticorps LOC100116446, anticorps Myo7a

Sujet: This gene 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. This gene encodes an unconventional myosin with a very short tail. Defects in this gene 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.

NCBI Accession: NP_000251

Pathways: Sensory Perception of Sound