Myosin VIIA anticorps (AA 850-1150)

N° du produit ABIN6144293

L’anticorps Lapin Polyclonal anti-Myosin VIIA a été validé pour WB. Il convient pour détecter Myosin VIIA dans des échantillons de Humain.

Aperçu rapide pour Myosin VIIA anticorps (AA 850-1150) (ABIN6144293)

Antigène: Myosin VIIA (MYO7A)

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Myosin VIIA est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-Myosin VIIA anticorps

Épitope: AA 850-1150

Séquence: MIARRLHQRL RAEYLWRLEA EKMRLAEEEK LRKEMSAKKA KEEAERKHQE RLAQLAREDA ERELKEKEAA RRKKELLEQM ERARHEPVNH SDMVDKMFGF LGTSGGLPGQ EGQAPSGFED LERGRREMVE EDLDAALPLP DEDEEDLSEY KFAKFAATYF QGTTTHSYTR RPLKQPLLYH DDEGDQLAAL AVWITILRFM GDLPEPKYHT AMSDGSEKIP VMTKIYETLG KKTYKRELQA LQGEGEAQLP EGQKKSSVRH KLVHLTLKKK SKLTEEVTKR LHDGESTVQG NSMLEDRPTS N

Réactivité croisée: Humain, Souris, Rat

Attributs du produit: Polyclonal Antibodies

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 850-1150 of human MYO7A (NP_000251.3).

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

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

Détails sur Myosin VIIA

Antigène: Myosin VIIA (MYO7A)

Autre désignation: 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.,MYO7A,DFNA11,DFNB2,MYOVIIA,MYU7A,NSRD2,USH1B,Signal Transduction,Cell Biology & Developmental Biology,Cytoskeleton,Motor Proteins,MYO7A

Poids moléculaire: 138 kDa/240 kDa/249 kDa/250 kDa/254 kDa

ID gène: 4647

UniProt: Q13402

Pathways: Sensory Perception of Sound