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RPGRIP1L antibody (AA 608-1264)

The Rabbit Polyclonal anti-RPGRIP1L antibody (ABIN7876102) specifically detects RPGRIP1L in WB, ELISA and FACS. The antibody is reactive with Human, Mouse and Rat samples.
Catalog No. ABIN7876102
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for RPGRIP1L antibody (AA 608-1264) (ABIN7876102)

Target

See all RPGRIP1L Antibodies
RPGRIP1L (RPGRIP1-Like (RPGRIP1L))

Reactivity

Human, Mouse, Rat

Host

  • 21
  • 1
Rabbit

Clonality

  • 22
Polyclonal

Conjugate

  • 8
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This RPGRIP1L antibody is un-conjugated

Application

  • 21
  • 13
  • 13
  • 7
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS)
  • Binding Specificity

    • 15
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 608-1264

    Purpose

    RPGRIP1L Antibody / Protein fantom

    Purification

    Antigen affinity purified

    Immunogen

    E. coli-derived recombinant human protein (amino acids E608-D1264) was used as the immunogen for the RPGRIP1L antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the RPGRIP1L 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 RPGRIP1L 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

    RPGRIP1L (RPGRIP1-Like (RPGRIP1L))

    Alternative Name

    RPGRIP1L

    Background

    The protein encoded by this gene can localize to the basal body-centrosome complex or to primary cilia and centrosomes in ciliated cells. The encoded protein has been found to interact with nephrocystin-4. Defects in this gene are a cause of Joubert syndrome type 7 (JBTS7) and Meckel syndrome type 5 (MKS5).

    UniProt

    Q68CZ1

    Pathways

    DNA Replication, Regulation of G-Protein Coupled Receptor Protein Signaling, Synthesis of DNA
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