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MYL3/CMLC1 antibody (AA 1-195)

This Rabbit Polyclonal antibody specifically detects MYL3/CMLC1 in WB and IF. It exhibits reactivity toward Human.
Catalog No. ABIN6144249

Quick Overview for MYL3/CMLC1 antibody (AA 1-195) (ABIN6144249)

Target

See all MYL3/CMLC1 (MYL3) Antibodies
MYL3/CMLC1 (MYL3) (Myosin, Light Chain 3 (MYL3))

Reactivity

  • 40
  • 11
  • 10
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 36
  • 6
Rabbit

Clonality

  • 37
  • 4
Polyclonal

Conjugate

  • 30
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This MYL3/CMLC1 antibody is un-conjugated

Application

  • 34
  • 21
  • 20
  • 5
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF)
  • Binding Specificity

    • 9
    • 5
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-195

    Sequence

    MAPKKPEPKK DDAKAAPKAA PAPAPPPEPE RPKEVEFDAS KIKIEFTPEQ IEEFKEAFML FDRTPKCEMK ITYGQCGDVL RALGQNPTQA EVLRVLGKPR QEELNTKMMD FETFLPMLQH ISKNKDTGTY EDFVEGLRVF DKEGNGTVMG AELRHVLATL GERLTEDEVE KLMAGQEDSN GCINYEAFVK HIMSS

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 1-195 of human MYL3 (NP_000249.1).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000,IF,1:50 - 1:200

    Comment

    HIGH QUALITY

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    MYL3/CMLC1 (MYL3) (Myosin, Light Chain 3 (MYL3))

    Alternative Name

    MYL3

    Background

    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.,MYL3,CMH8,MLC-lV/sb,MLC1SB,MLC1V,VLC1,VLCl,Signal Transduction,Cell Biology & Developmental Biology,Cytoskeleton,Motor Proteins,Actins,Cardiovascular,Heart,Contractility,MYL3

    Molecular Weight

    21 kDa

    Gene ID

    4634

    UniProt

    P08590
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