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RNF59/MID1 Polyclonal Antibody

Applications

  • WB
  • IHC-P
  • IF(IHC-P)

Reactivity

  • Rat

Predicted Reactivity

  • Human
  • Mouse
  • Dog
  • Sheep
  • Pig
  • Horse
  • Chicken
Overview
Catalog # bs-9380R
Product Name RNF59/MID1 Polyclonal Antibody
Applications WB, IHC-P, IF(IHC-P)
Reactivity Rat
Predicted Reactivity Human, Mouse, Dog, Sheep, Pig, Horse, Chicken
Specifications
Conjugation Unconjugated
Host Rabbit
Source KLH conjugated synthetic peptide derived from human Midline-1/RNF59
Clonality Polyclonal
Clone # #REF!
Isotype IgG
Concentration 1ug/ul
Purification Purified by Protein A.
Storage Buffer 0.01M TBS(pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Storage Condition Shipped at 4_. Store at -20_ for one year. Avoid repeated freeze/thaw cycles.
Target
Gene ID 4281
Swiss Prot O15344
Synonyms BBBG1; Finger on X and Y mouse homolog of antibody; FXY; GBBB1; MID-1; Mid1; Midin; Midline 1 Opitz/BBB syndrome; Midline 1; Midline 1 ring finger; Midline 1 RING finger protein; Midline-1; Midline1; OGS1; OSX; Putative transcription factor XPRF; RING finger protein 59; RNF59; TRI18; TRI18_HUMAN; TRIM18; Tripartite mot containing protein 18; Tripartite mot protein TRIM18; Tripartite mot-containing protein 18; XPRF; Zinc finger X and Y antibody; ZNFXY.
Background 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 characterized 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.
Application Dilution
WB 1:300-5000
IHC-P 1:200-400
IF(IHC-P) 1:50-200