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Myosin Heavy Chain, Smooth Muscle (SMMHC) (PT0275R) rabbit mAb

Product code: YP-Ab-18155
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Product introduction

Reactive species
Human;Mouse;(predicted: Rat)
Applications
WB;IHC; ELISA
Antibody type
Monoclonal antibodies
Gene Name
MYH11
Protein name
Myosin Heavy Chain, Smooth Muscle
Dalton(DA)
227kD
Immunogen
Synthesized peptide derived from human Myosin Heavy Chain, Smooth Muscle AA range:300-400
Specificity
This antibody detects endogenous levels of Myosin Heavy Chain, Smooth Muscle
Constitute
PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
Source
Monoclonal, Rabbit IgG1, Kappa
Dilution rate
IHC 1:100-500, WB 1:500-1000, ELISA 1:5000-20000
Purification process
Recombinant Expression and Affinity purified
Concentration
mg/ml
Stockpile
-15°C to -25°C/1 year(Do not lower than -25°C)
Other name
AAT4;DKFZp686D10126;DKFZp686D19237;FAA4;FLJ35232;MGC126726;MGC32963;MYH 11;MYH11;MYH11_HUMAN;Myosin 11;Myosin heavy chain 11;Myosin heavy chain 11 smooth muscle;Myosin heavy chain;Myosin heavy chain smooth muscle isoform;Myosin heavy polypeptide 11 smooth muscle;Myosin-11;SMHC;SMMHC;smooth muscle isoform;Smooth muscle myosin heavy chain 11 isoform SM2;Smooth muscle myosin heavy chain isoform SM2
Background
The protein encoded by this gene is a smooth muscle myosin belonging to the myosin heavy chain family. The gene product is a subunit of a hexameric protein that consists of two heavy chain subunits and two pairs of non-identical light chain subunits. It functions as a major contractile protein, converting chemical energy into mechanical energy through the hydrolysis of ATP. The gene encoding a human ortholog of rat NUDE1 is transcribed from the reverse strand of this gene, and its 3' end overlaps with that of the latter. The pericentric inversion of chromosome 16 [inv(16)(p13q22)] produces a chimeric transcript that encodes a protein consisting of the first 165 residues from the N terminus of core-binding factor beta in a fusion with the C-terminal portion of the smooth muscle myosin heavy chain. This chromosomal rearrangement is associated with acute myeloid leukemia of the M4Eo subtype. Alter
Function
disease:A chromosomal aberr

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