MYL3 purified MaxPab rabbit polyclonal antibody (D01P)

Catalog # H00004634-D01P

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Size:100 ug
Price: USD $ 376.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
Western Blot (Transfected lysate)
Application

Western Blot (Transfected lysate)

Western Blot analysis of MYL3 expression in transfected 293T cell line (H00004634-T02) by MYL3 MaxPab polyclonal antibody.

Lane 1: MYL3 transfected lysate(21.90 KDa).
Lane 2: Non-transfected lysate.

  • Specification

    Product Description

    Rabbit polyclonal antibody raised against a full-length human MYL3 protein.MaxPab Polyclonal Antibody,MaxPab Polyclonal Antibodies,MaxPab,DNA Immune,DNA Immunization,Immune Technology

    Immunogen

    MYL3 (NP_000249.1, 1 a.a. ~ 195 a.a) full-length human protein.

    Sequence

    MAPKKPEPKKDDAKAAPKAAPAPAPPPEPERPKEVEFDASKIKIEFTPEQIEEFKEAFMLFDRTPKCEMKITYGQCGDVLRALGQNPTQAEVLRVLGKPRQEELNTKMMDFETFLPMLQHISKNKDTGTYEDFVEGLRVFDKEGNGTVMGAELRHVLATLGERLTEDEVEKLMAGQEDSNGCINYEAFVKHIMSS

    Host

    Rabbit

    Reactivity

    Human

    Quality Control Testing

    Antibody reactive against mammalian transfected lysate.

    Storage Buffer

    In 1x PBS, pH 7.4

    Storage Instruction

    Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.

  • Applications

    Western Blot (Transfected lysate)

    Western Blot analysis of MYL3 expression in transfected 293T cell line (H00004634-T02) by MYL3 MaxPab polyclonal antibody.

    Lane 1: MYL3 transfected lysate(21.90 KDa).
    Lane 2: Non-transfected lysate.
  • Gene Info — MYL3

    Entrez GeneID

    4634

    GeneBank Accession#

    NM_000258.1

    Protein Accession#

    NP_000249.1

    Gene Name

    MYL3

    Gene Alias

    CMH8, MLC1SB, MLC1V, VLC1

    Gene Description

    myosin, light chain 3, alkali; ventricular, skeletal, slow

    Omim ID

    160790 608751

    Gene Ontology

    Hyperlink

    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

  • Interactome
  • Pathway
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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