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Last updated: 2016/12/4

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MYL3 (Human) Recombinant Protein (P01)

  • Catalog # : H00004634-P01
  • Visit Frequency :
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  • Specification
  • Product Description:
  • Human MYL3 full-length ORF ( AAH09790, 1 a.a. - 195 a.a.) recombinant protein with GST-tag at N-terminal.
  • Sequence:
  • MAPKKPEPKKDDAKAAPKAAPAPAPPPEPERPKEVEFDASKIKIEFTPEQIEEFKEAFMLFDRTPKCEMKITYGQCGDVLRALGQNPTQAEVLRVLGKPRQEELNTKMMDFETFLPMLQHISKNKDTGTYEDFVEGLRVFDKEGNGTVMGAELRHVLATLGERLTEDEVEKLMAGQEDSNGCINYEAFVKHIMSS
  • Host:
  • Wheat Germ (in vitro)
  • Theoretical MW (kDa):
  • 47.19
  • Purification:
  • Glutathione Sepharose 4 Fast Flow
  • Quality Control Testing:
  • 12.5% SDS-PAGE Stained with Coomassie Blue.

    QC Testing of H00004634-P01
  • Storage Buffer:
  • 50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer.
  • Storage Instruction:
  • Store at -80°C. Aliquot to avoid repeated freezing and thawing.
  • Note:
  • Best use within three months from the date of receipt of this protein.
  • Applications
  • Enzyme-linked Immunoabsorbent Assay
  • Western Blot (Recombinant protein)
  • Antibody Production
  • Protein Array
  • Application Image
  • Enzyme-linked Immunoabsorbent Assay
  • Western Blot (Recombinant protein)
  • Antibody Production
  • Protein Array
  • Gene Information
  • Entrez GeneID:
  • 4634
  • Gene Name:
  • MYL3
  • Gene Alias:
  • CMH8,MLC1SB,MLC1V,VLC1
  • Gene Description:
  • myosin, light chain 3, alkali; ventricular, skeletal, slow
  • Gene Summary:
  • MYL3 encodes myosin light chain 3, an alkali light chain also referred to in the literature as both the ventricular isoform and the slow skeletal muscle isoform. Mutations in MYL3 have been identified as a cause of mid-left ventricular chamber type hypertrophic cardiomyopathy. [provided by RefSeq
  • Other Designations:
  • OTTHUMP00000165922,myosin, light polypeptide 3, alkali; ventricular, skeletal, slow,slow skeletal ventricular myosin alkali light chain 3
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