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OFD1 antibody (AA 136-387 of Human)

OFD1 Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN1886022
  • Target See all OFD1 Antibodies
    OFD1 (Oral-Facial-Digital Syndrome 1 (OFD1))
    Binding Specificity
    • 6
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 136-387 of Human
    Reactivity
    • 12
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Human
    Host
    • 12
    Rabbit
    Clonality
    • 12
    Polyclonal
    Conjugate
    • 8
    • 2
    • 1
    • 1
    This OFD1 antibody is un-conjugated
    Application
    • 8
    • 5
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Purification
    Purified by antigen-affinity chromatography.
    Immunogen
    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 136 and 387 of Human OFD1
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    Discover our top product OFD1 Primary Antibody
  • Application Notes
    Suggested dilutions:
    Western blotting: 1.500-1.3000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.
    Preservative
    Thimerosal (Merthiolate)
    Precaution of Use
    Biohazard Informations: This product contains thimerosal which is hazardous.
    Storage
    4 °C/-20 °C
    Storage Comment
    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • Target
    OFD1 (Oral-Facial-Digital Syndrome 1 (OFD1))
    Alternative Name
    oral-facial-digital syndrome 1 (OFD1 Products)
    Synonyms
    71-7A antibody, CXorf5 antibody, JBTS10 antibody, RP23 antibody, SGBS2 antibody, RGD1562231 antibody, OFD1, centriole and centriolar satellite protein antibody, OFD1 antibody, ofd1 antibody, Ofd1 antibody
    Background
    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.Alternatively spliced transcripts have been described for this gene but the biological validity of these transcripts has not been determined.[provided by RefSeq]
    Molecular Weight
    117 kDa
    Gene ID
    8481
    NCBI Accession
    NM_003611, NP_003602
    Pathways
    M Phase
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