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Anti-Midline-1 Rabbit Polyclonal Antibody (Alexa Fluor® 750)
  BOSSBS-9380R-A750
 :  Bioss
Anti-Midline-1 Rabbit Polyclonal Antibody (Alexa Fluor® 750)
  BOSSBS-9380R-A750
 :  Bioss

 

  • Antibody type:
    Primary
  • Antigen name:
    Midline-1
  • Clonality:
    Polyclonal
  • Conjugation:
    Alexa Fluor® 750
  • Host:
    Rabbit
  • ImmunoChemistry:
    Yes
  • ImmunoFluorescence:
    Yes
  • Isotype:
    IgG
  • Reactivity:
    Human,
    Rat,
    Mouse
  • Western blot:
    Yes
  • Environmentally Preferable:
  • Epitope:
    171-270/667
  • Form:
    Liquid
  • Gene ID:
    4281
  • Antigen synonyms:
    Midline 1 Opitz/BBB syndrome|GBBB1|ZNFXY|Midline 1|Midline-1|OSX|Midline 1 RING finger protein|Mid1|Tripartite mot protein TRIM18|Tripartite mot containing protein 18|Finger on X and Y mouse homolog of antibody|XPRF|BBBG1|TRI18_HUMAN|Midline 1 ring finger|TRIM18|Tripartite mot-containing protein 18|Midin|TRI18|Midline1|Putative transcription factor XPRF|OGS1|Zinc finger X and Y antibody|RING finger protein 59|RNF59|MID-1|FXY
  • Modification:
    Unmodified
  • Storage buffer:
    Aqueous buffered solution containing 0,01 M TBS (pH 7,4) with 1% BSA, 0,03% Proclin300 and 50% Glycerol
  • Storage temperature:
    Store at ‒20 °C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
  • Concentration:
    1 µg/µl
  • Shipping temperature:
    4 °C
  • Immunogen:
    KLH conjugated synthetic peptide derived from human Midline-1/RNF59
  • Purification:
    Purified by Protein A
  • Pack type:
    Vial
  • Pk:
    100 µl

 

 

Midline-1 (Tripartite motif-containing protein 18, Putative transcription factor XPRF, RING finger protein 59) is a 667 amino acid protein encoded by the human gene MID1. Midline-1 belongs to the TRIM/RBCC family and contains two B box-type zinc fingers, one B30.2/SPRY domain, one COS domain, one fibronectin type-III domain and one RING-type zinc finger. Midline-1 is believed to have E3 ubiquitin ligase activity which targets the catalytic subunit of protein phosphatase 2 for degradation. It is a cytoplasmic protein found as a homodimer or heterodimer with Midline-2. It also interacts with IGBP1 (Lymphocyte signaling protein A4). Defects in MID1 are the cause of Opitz syndrome type I (OS-I). OS-I is an X-linked recessive disorder characterised by hypertelorism, genital-urinary defects such as hypospadias in males and splayed labia in females, lip-palate-laryngotracheal clefts, imperforate anus, developmental delay and congenital heart defects. OS-I mutations produce proteins with a decreased affinity for microtubules.

Type: Primary
Antigen: Midline-1
Clonality: Polyclonal
Clone:
Conjugation: ALEXA FLUOR® 750
Public Immunogen Range: 171-270/667
Host: Rabbit
Isotype: IgG
Reactivity: Human; Mouse; Rat