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T80 (THVGP103) (AA 51-150) antibody

This anti- antibody is a Rabbit Polyclonal antibody detecting in ELISA, ICC, IF (cc), IF (p), IHC (fro), IHC (p) and WB. Suitable for Human.
Catalog No. ABIN1714839

Quick Overview for T80 (THVGP103) (AA 51-150) antibody (ABIN1714839)

Target

T80 (THVGP103)

Reactivity

Human

Host

Rabbit

Clonality

Polyclonal

Application

ELISA, Immunocytochemistry (ICC), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Western Blotting (WB)
  • Binding Specificity

    AA 51-150

    Predicted Reactivity

    Human,Mouse,Rat,Dog,Cow,Pig,Rabbit

    Purification

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human IFT80

    Isotype

    IgG
  • Application Notes

    WB 1:300-5000
    ELISA 1:500-1000
    IHC-P 1:200-400
    IHC-F 1:100-500
    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200
    ICC 1:100-500

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

    Preservative

    ProClin

    Precaution of Use

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

    Storage

    4 °C,-20 °C

    Storage Comment

    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

    Expiry Date

    12 months
  • Target

    T80 (THVGP103)

    Alternative Name

    T80

    Background

    Synonyms: ATD2, t80, T80_HUMAN, Intraflagellar transport 80 homolog Chlamydomonas, Intraflagellar transport protein 80 homolog, KIAA1374, WD repeat domain 56, WD repeat-containing protein 56, WDR56.

    Background: IFT80 is a encoded by this gene is part of the intraflagellar transport complex B and is necessary for the function of motile and sensory cilia. Defects in this gene are a cause of asphyxiating thoracic dystrophy 2 (ATD2). Three transcript variants encoding two different isoforms have been found for this gene.

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