MYH9 Rabbit Monoclonal antibody

MYH9 Rabbit Monoclonal antibody

Cat: AMRe03116
Size:50μL Price:168 $99
Size:100μL Price:300 $180
Application:WB,IHC,IP

Reactivity:Human,Rat
Conjugate:Unconjugated
Optional conjugates: Biotin, FITC (free of charge).
See other 26 conjugates.

Gene Name:MYH9
Category: 組換えモノクローナル抗体 Tags: , , , , , , , ,

Summary

Production Name

MYH9 Rabbit Monoclonal antibody

Description

Recombinant rabbit monoclonal antibody

Host

Rabbit

Application

WB,IHC,IP

Reactivity

Human,Rat

 

Performance

Conjugation

Unconjugated

Modification

Unmodified

Isotype

IgG

Clonality

Monoclonal Antibody

Form

Liquid

Storage

Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.

Buffer

50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.01% Sodium azide and 0.05% protective protein

Purification

Affinity Purified

 

Immunogen

Gene Name

MYH9

Alternative Names

MHA; FTNS; EPSTS; BDPLT6; DFNA17; MATINS; NMMHCA; NMHC-II-A; NMMHC-IIA

Gene ID

4627

SwissProt ID

P35579

 

Application

Dilution Ratio

WB 1:500-1:1000,IHC 1:50-1:100,IP 1:20-1:50

Molecular Weight

Calculated MW: 227 kDa; Observed MW: 227 kDa

 

Background

This gene encodes a conventional non-muscle myosin; this protein should not be confused with the unconventional myosin-9a or 9b (MYO9A or MYO9B). The encoded protein is a myosin IIA heavy chain that contains an IQ domain and a myosin head-like domain which is involved in several important functions, including cytokinesis, cell motility and maintenance of cell shape. Defects in this gene have been associated with non-syndromic sensorineural deafness autosomal dominant type 17, Epstein syndrome, Alport syndrome with macrothrombocytopenia, Sebastian syndrome, Fechtner syndrome and macrothrombocytopenia with progressive sensorineural deafness. [provided by RefSeq, Dec 2011]

 

Research Area

Signal Transduction

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