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OFD1 antibody

The Rabbit Polyclonal anti-OFD1 antibody (ABIN7881878) specifically detects OFD1 in WB, IF and FACS. The antibody is reactive with Human, Mouse and Rat samples.
Catalog No. ABIN7881878
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for OFD1 antibody (ABIN7881878)

Target

See all OFD1 Antibodies
OFD1 (Oral-Facial-Digital Syndrome 1 (OFD1))

Reactivity

  • 17
  • 6
  • 4
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 17
Rabbit

Clonality

  • 17
Polyclonal

Conjugate

  • 13
  • 2
  • 1
  • 1
This OFD1 antibody is un-conjugated

Application

  • 12
  • 7
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF), Flow Cytometry (FACS)
  • Purpose

    OFD1 Antibody / Oral-facial-digital syndrome 1

    Sequence

    KDKSAHSENP LEKYMKIIQQ EQDQESADK

    Purification

    Affinity purified

    Immunogen

    Amino acids KDKSAHSENPLEKYMKIIQQEQDQESADK from the human protein were used as the immunogen for the OFD1 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the OFD1 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 OFD1 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

    OFD1 (Oral-Facial-Digital Syndrome 1 (OFD1))

    Alternative Name

    OFD1

    Background

    Oral-facial-digital syndrome 1 protein is a protein that in humans is encoded by the OFD1 gene. This gene is mapped to Xp22.2. This gene is located on the X chromosome and encodes a centrosomal protein. A knockout mouse model has been used to study the effect of mutations in this gene. The mouse gene is also located on the X chromosome, however, unlike the human gene it is not subject to X inactivation. Mutations in this gene are associated with oral-facial-digital syndrome type I and Simpson-Golabi-Behmel syndrome type 2. Many pseudogenes have been identified, a single pseudogene is found on chromosome 5 while as many as fifteen have been found on the Y chromosome.

    UniProt

    O75665

    Pathways

    M Phase
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