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ARL13B antibody (AA 16-428)

The Rabbit Polyclonal anti-ARL13B antibody (ABIN7871077) specifically detects ARL13B in WB, ELISA, IF, IHC (p) and FACS. The antibody is reactive with Human, Mouse and Rat samples.
Catalog No. ABIN7871077
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for ARL13B antibody (AA 16-428) (ABIN7871077)

Target

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

Reactivity

  • 15
  • 14
  • 6
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

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  • 11
Rabbit

Clonality

  • 13
  • 11
Polyclonal

Conjugate

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  • 1
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  • 1
This ARL13B antibody is un-conjugated

Application

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  • 10
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  • 7
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)
  • Binding Specificity

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    • 2
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    AA 16-428

    Purpose

    ARL13B Antibody / ADP-ribosylation factor-like protein 13B

    Purification

    Antigen affinity purified

    Immunogen

    Recombinant human protein (amino acids R16-S428) was used as the immunogen for the ARL13B antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the ARL13B antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the ARL13B antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

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

    Alternative Name

    ARL13B

    Background

    ADP-ribosylation factor-like protein 13B (ARL13B), also known as ADP-ribosylation factor-like protein 2-like 1 (ARL2L1), is a protein that in humans is encoded by the ARL13B gene. 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.

    UniProt

    Q3SXY8
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