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ARL13B antibody

The Rabbit Polyclonal anti-ARL13B antibody has been validated for WB, IF, ICC and IHC (p). It is suitable to detect ARL13B in samples from Human.
Catalog No. ABIN7467937

Quick Overview for ARL13B antibody (ABIN7467937)

Target

See all ARL13B Antibodies
ARL13B (ADP-Ribosylation Factor-Like 13B (ARL13B))

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This ARL13B antibody is un-conjugated

Application

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Western Blotting (WB), Immunofluorescence (IF), Immunocytochemistry (ICC), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Cross-Reactivity

    Human, Mouse, Rat

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein encompassing a sequence within the center region of human ARL13B. The exact sequence is proprietary.

    Isotype

    IgG
  • Application Notes

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

    Comment

    Positive Control: Mouse liver Validation: Orthogonal

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    0.1M Tris-Glycine ( pH 7), 20 % Glycerol, 0.01 % Thimerosal

    Preservative

    Thimerosal (Merthiolate)

    Precaution of Use

    This product contains Thimerosal (Merthiolate): 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

    ARL13B (ADP-Ribosylation Factor-Like 13B (ARL13B))

    Alternative Name

    ADP ribosylation factor like GTPase 13B

    Background

    Synonyms: ADP ribosylation factor like GTPase 13B , ARL2L1 , JBTS8

    Background: This gene encodes a member of the ADP-ribosylation factor-like family. The encoded protein is a small GTPase that contains both N-terminal and C-terminal guanine nucleotide-binding motifs. This protein is localized in the cilia and plays a role in cilia formation and in maintenance of cilia. Mutations in this gene are the cause of Joubert syndrome 8. Alternate splicing results in multiple transcript variants. [provided by RefSeq]

    Molecular Weight

    49 kDa

    Gene ID

    200894

    UniProt

    Q3SXY8
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