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FTL antibody

The Rabbit Polyclonal anti-FTL antibody has been validated for WB, IHC, ELISA and IF. It is suitable to detect FTL in samples from Human and Mouse.
Catalog No. ABIN7114184

Quick Overview for FTL antibody (ABIN7114184)

Target

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

Reactivity

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  • 1
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Human, Mouse

Host

  • 89
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Rabbit

Clonality

  • 106
  • 71
Polyclonal

Conjugate

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  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
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  • 1
This FTL antibody is un-conjugated

Application

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Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF)
  • Purification

    Immunogen affinity purified

    Purity

    ≥95 % as determined by SDS-PAGE

    Immunogen

    ferritin, light polypeptide

    Isotype

    IgG
  • Application Notes

    WB: 1:500 - 1:2000, IHC: 1:50 - 1:200, IF: 1:10 - 1:100

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide and 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

    -20°C for 12 months (Avoid repeated freeze / thaw cycles.)

    Expiry Date

    12 months
  • Target

    FTL (Ferritin, Light Polypeptide (FTL))

    Alternative Name

    Ferritin light chain

    Background

    Synonyms:Ferritin L subunit, Ferritin light chain, ferritin, light polypeptide, 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

    18 kDa

    Gene ID

    2512

    UniProt

    P02792

    Pathways

    Transition Metal Ion Homeostasis
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