
Thermo Fisher Scientific MID1 Polyclonal Antibody
Rabbit polyclonal antibody targeting human MID1 protein for WB, IHC, and ICC applications. Recognizes internal region peptide of TRI18. Unconjugated liquid form with 1 mg/mL concentration, suitable for research use only.
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Thermo Fisher Scientific MID1 Polyclonal Antibody
Applications and Tested Dilution
| Application | Tested Dilution |
|---|---|
| Western Blot (WB) | 1:500–1:1,000 |
| Immunohistochemistry (Paraffin) (IHC (P)) | 1:50–1:100 |
| Immunocytochemistry (ICC/IF) | 1:100–1:500 |
Product Specifications
| Specification | Description |
|---|---|
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Synthetic peptide derived from the internal region of human TRI18 |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 1 mg/mL |
| Storage Conditions | -20°C |
| Shipping Conditions | Wet ice |
| RRID | AB_2555123 |
Target Information
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
- One RING-type zinc finger
Midline-1 is believed to have E3 ubiquitin ligase activity targeting the catalytic subunit of protein phosphatase 2 for degradation. It is a cytoplasmic protein found as a homodimer or heterodimer with Midline-2 and interacts with IGBP1 (Lymphocyte signaling protein A4).
Defects in MID1 cause Opitz syndrome type I (OS-I), an X-linked recessive disorder characterized by:
- Hypertelorism
- Genital-urinary defects (e.g., hypospadias in males, splayed labia in females)
- Lip-palate-laryngotracheal clefts
- Imperforate anus
- Developmental delay
- Congenital heart defects
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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