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FTL Protein (Myc-DYKDDDDK Tag)

This Recombinant FTL protein is produced in HEK-293 Cells.
Catalog No. ABIN2721021
$956.40
Plus shipping costs $50.00, if applicable $20.00 dry ice
20 μg
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Delivery in 11 to 12 Business Days

Quick Overview for FTL Protein (Myc-DYKDDDDK Tag) (ABIN2721021)

Target

See all FTL Proteins
FTL (Ferritin, Light Polypeptide (FTL))

Protein Type

Recombinant

Origin

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Human

Source

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HEK-293 Cells

Application

Antibody Production (AbP), Standard (STD)

Purity

> 80 % as determined by SDS-PAGE and Coomassie blue staining
  • Purification tag / Conjugate

    This FTL protein is labelled with Myc-DYKDDDDK Tag.

    Characteristics

    • Recombinant human Ferritin light chain (FTL) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
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  • Application Notes

    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays

    Comment

    The tag is located at the C-terminal.

    Restrictions

    For Research Use only
  • Concentration

    50 μg/mL

    Buffer

    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

    Storage

    -80 °C

    Storage Comment

    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • Target

    FTL (Ferritin, Light Polypeptide (FTL))

    Alternative Name

    Ferritin Light Chain (Ftl)

    Background

    This gene encodes the light subunit of the ferritin protein. Ferritin is the major intracellular iron storage protein in prokaryotes and eukaryotes. It is composed of 24 subunits of the heavy and light ferritin chains. Variation in ferritin subunit composition may affect the rates of iron uptake and release in different tissues. A major function of ferritin is the storage of iron in a soluble and nontoxic state. Defects in this light chain ferritin gene are associated with several neurodegenerative diseases and hyperferritinemia-cataract syndrome. This gene has multiple pseudogenes.

    Molecular Weight

    19.8 kDa

    NCBI Accession

    NP_000137

    Pathways

    Transition Metal Ion Homeostasis
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