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ATL1 antibody

This anti-ATL1 antibody is a Rabbit Polyclonal antibody detecting ATL1 in WB, IF and ICC. Suitable for Human.
Catalog No. ABIN7467878

Quick Overview for ATL1 antibody (ABIN7467878)

Target

See all ATL1 Antibodies
ATL1 (Atlastin GTPase 1 (ATL1))

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This ATL1 antibody is un-conjugated

Application

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Western Blotting (WB), Immunofluorescence (IF), Immunocytochemistry (ICC)
  • Cross-Reactivity

    Human, Mouse, Rat

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein encompassing a sequence within the center region of human ATL1. The exact sequence is proprietary.

    Isotype

    IgG
  • Application Notes

    WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1.31 mg/mL

    Buffer

    1XPBS pH 7, 20 % Glycerol, 0.025 % ProClin 300

    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

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • Target

    ATL1 (Atlastin GTPase 1 (ATL1))

    Alternative Name

    atlastin GTPase 1

    Background

    Atlastin GTPase 1 , AD-FSP , FSP1 , GBP3 , HSN1D , SPG3 , SPG3A , atlastin1,The protein encoded by this gene is a GTPase and a Golgi body transmembrane protein. The encoded protein can form a homotetramer and has been shown to interact with spastin and with mitogen-activated protein kinase kinase kinase kinase 4. This protein may be involved in axonal maintenance as evidenced by the fact that defects in this gene are a cause of spastic paraplegia type 3. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq]

    Molecular Weight

    64 kDa

    Gene ID

    51062

    UniProt

    Q8WXF7
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