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MYO1A Polyclonal Antibody
MYO1A Polyclonal Antibody
Origin of place China
Model ABP59374
Supplier Abbkine Scientific
Price
Hits 88
Updated 10/16/2019
  • Product Detail
  • Company Profile

MYO1A (Myosin IA) is a Protein Coding gene. Diseases associated with MYO1A include Dfna48 Nonsyndromic Hearing Loss And Deafness and Deafness, Autosomal Dominant 48. Among its related pathways are Sertoli-Sertoli Cell Junction Dynamics and Actin Nucleation by ARP-WASP Complex. MYO1A encodes a member of the myosin superfamily. The protein represents an unconventional myosin; it should not be confused with the conventional skeletal muscle myosin-1 (MYH1). Unconventional myosins contain the basic domains characteristic of conventional myosins and are further distinguished from class members by their tail domains. They function as actin-based molecular motors.

Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000 ELISA 1:5000-20000.

MYO1A Polyclonal Antibody product listed herein is for research use only and is not intended for use in human or clinical diagnosis. Suggested applications of our products are not recommendations to use our products in violation of any patent or as a license. We cannot be responsible for patent infringements or other violations that may occur with the use of this product.

Find more details at https://www.abbkine.com/product/myo1a-polyclonal-antibody-abp59374/

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