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IHC-P analysis of human kidney tissue using GTX04955 MID1 antibody. Antigen retrieval : Heat mediated antigen retrieval with citrate buffer. Dilution : 1:100
IHC-P analysis of human kidney tissue using GTX04955 MID1 antibody. Antigen retrieval : Heat mediated antigen retrieval with citrate buffer. Dilution : 1:100
IHC-P analysis of human kidney tissue using GTX04955 MID1 antibody. Antigen retrieval : Heat mediated antigen retrieval with citrate buffer. Dilution : 1:100

Midline-1 antibody

GTX04955
GeneTex
ApplicationsWestern Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman
TargetMID1
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Overview

  • Supplier
    GeneTex
  • Product Name
    MID1 antibody
  • Delivery Days Customer
    7
  • Application Supplier Note
    WB: 1:500-1:3000. IHC-P: 1:50-1:200. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID4281
  • Target name
    MID1
  • Target description
    midline 1
  • Target synonyms
    BBBG1; E3 ubiquitin-protein ligase Midline-1; FXY; GBBB1; MIDIN; midline 1 RING finger protein; OGS1; Opitz/BBB syndrome; OS; OSX; putative transcription factor XPRF; RING finger protein 59; RING finger protein Midline-1; RING-type E3 ubiquitin transferase Midline-1; RNF59; TRIM18; tripartite motif protein TRIM18; tripartite motif-containing protein 18; XPRF; zinc finger on X and Y, mouse, homolog of; ZNFXY
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDO15344
  • Protein Name
    E3 ubiquitin-protein ligase Midline-1
  • Scientific Description
    The protein encoded by this gene is a member of the tripartite motif (TRIM) family, also known as the RING-B box-coiled coil (RBCC) subgroup of RING finger proteins. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein forms homodimers which associate with microtubules in the cytoplasm. The protein is likely involved in the formation of multiprotein structures acting as anchor points to microtubules. Mutations in this gene have been associated with the X-linked form of Opitz syndrome, which is characterized by midline abnormalities such as cleft lip, laryngeal cleft, heart defects, hypospadias, and agenesis of the corpus callosum. This gene was also the first example of a gene subject to X inactivation in human while escaping it in mouse. Alternative promoter use, alternative splicing and alternative polyadenylation result in multiple transcript variants that have different tissue specificities. [provided by RefSeq, Dec 2016]
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203