MYH9 Rabbit Monoclonal antibody

MYH9 Rabbit Monoclonal antibody

SKU: AMRe03116
Size1:50μL Price1:$188 $99
Size2:100μL Price2:$338 $180

Application:WB,IHC-P,IP

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

Gene Name:MYH9 Category: Recombinant Monoclonal Antibody Tags: , , , , , , , ,

Summary

Production Name

MYH9 Rabbit Monoclonal antibody

Description

Recombinant Rabbit Monoclonal antibody

Host

Rabbit

Application

WB,IHC-P,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

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