OFD1 polyclonal antibody

Catalog # PAB22773

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Size:100 uL
Price: USD $ 428.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Application

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)

Immunohistochemical staining of human liver with OFD1 polyclonal antibody (Cat # PAB22773) shows strong cytoplasmic positivity in hepatocytes at 1:200-1:500 dilution.

  • Specification

    Product Description

    Rabbit polyclonal antibody raised against recombinant OFD1.

    Immunogen

    Recombinant protein corresponding to amino acids of human OFD1.

    Sequence

    TALENEVYCNPKQSVIDRSVNGLINGNVVPCNGEISGDFLNNPFKQENVLARMVASRITNYPTAWVEGSSPDSDLEFVANTK

    Host

    Rabbit

    Reactivity

    Human

    Form

    Liquid

    Purification

    Antigen affinity purification

    Isotype

    IgG

    Recommend Usage

    Immunohistochemistry (1:200-1:500)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In PBS, pH 7.2 (40% glycerol, 0.02% sodium azide)

    Storage Instruction

    Store at 4°C. For long term storage store at -20°C.
    Aliquot to avoid repeated freezing and thawing.

    Note

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

  • Applications

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)

    Immunohistochemical staining of human liver with OFD1 polyclonal antibody (Cat # PAB22773) shows strong cytoplasmic positivity in hepatocytes at 1:200-1:500 dilution.
  • Gene Info — OFD1

    Entrez GeneID

    8481

    Protein Accession#

    O75665

    Gene Name

    OFD1

    Gene Alias

    71-7A, CXorf5, MGC117039, MGC117040, SGBS2

    Gene Description

    oral-facial-digital syndrome 1

    Omim ID

    300170 300209 311200

    Gene Ontology

    Hyperlink

    Gene Summary

    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

    Other Designations

    OTTHUMP00000022940

  • Interactome
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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