MYH7 Antibody (2021A) [Alexa Fluor® 532]

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Product Details

Summary
Reactivity HuSpecies Glossary
Applications WB, ICC/IF
Clone
2021A
Clonality
Monoclonal
Host
Rabbit
Conjugate
Alexa Fluor 532

Order Details

MYH7 Antibody (2021A) [Alexa Fluor® 532] Summary

Additional Information
Recombinant Monoclonal Antibody.
Immunogen
Human MYH7 synthetic peptide
Accession # P12883
Specificity
Detects human MYH7 in direct ELISAs and Western blots.
Isotype
IgG
Clonality
Monoclonal
Host
Rabbit
Purity Statement
Protein A or G purified
Innovator's Reward
Test in a species/application not listed above to receive a full credit towards a future purchase.

Applications/Dilutions

Dilutions
  • Immunocytochemistry
  • Western Blot

Packaging, Storage & Formulations

Storage
Protect from light. Do not freeze. 12 months from date of receipt, 2 to 8 °C as supplied
Buffer
Supplied 0.2mg/ml in 1X PBS with RDF1 and 0.09% Sodium Azide

Notes

This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.

Alternate Names for MYH7 Antibody (2021A) [Alexa Fluor® 532]

  • cardiac muscle beta isoform
  • CMD1S
  • CMD1SMGC138376
  • CMH1
  • DKFZp451F047
  • MGC138378
  • MPD1
  • MYH7
  • MYHCB
  • MyHC-beta
  • myhc-slow
  • myopathy, distal 1
  • myosin heavy chain (AA 1-96)
  • myosin, heavy chain 7, cardiac muscle, beta
  • myosin, heavy polypeptide 7, cardiac muscle, beta
  • Myosin-7
  • rhabdomyosarcoma antigen MU-RMS-40.7A
  • SPMD
  • SPMM

Background

MYH7 encodes the beta myosin heavy chain (MHC-beta ) which is a component of cardiac muscle myosin mainly expressed in the ventricle of fetal heart and represents the minority myosin in the adult heart. This is the 'slow form' of cardiac myosin as opposed to the 'fast form' (MYH6, aka MHC-alpha ) expressed more predominantely in the atria of the fetal heart and is the predominant myosin in the adult heart. The two isoforms of cardiac MHC alpha  and  beta  display 93% homology but have significantly different enzymatic properties, with  alpha  having 150-300% the contractile velocity and 60-70% actin attachment time as that of beta . Several mutations in MYH7 have been associated with inherited cardiomyopathies paraspinal and proximal muscle atrophy. MYH7 is a 223 kDa protein composed of 1935 amino acids.

Limitations

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

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