
Thermo Fisher Scientific MID1 Polyclonal Antibody
Human MID1 단백질을 표적으로 하는 Rabbit Polyclonal Antibody로 Western blot 및 Immunoprecipitation에 사용 가능. 항원 친화 크로마토그래피로 정제되었으며 액상 형태, 1 mg/mL 농도. 4°C 보관, 연구용 전용.
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Applications
| Application | Tested Dilution |
|---|---|
| Western Blot (WB) | 1:2,000–1:10,000 |
| Immunoprecipitation (IP) | Assay-dependent |
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Region between residue 617 and 667 of human midline 1 |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 1 mg/mL |
| Purification | Antigen affinity chromatography |
| Storage Buffer | Tris citrate/phosphate, pH 7–8 |
| Contains | 0.09% sodium azide |
| Storage Conditions | 4°C |
| Shipping Conditions | Wet ice |
Product Specific Information
- Recommended shelf life: 1 year from date of receipt
- Based on 100% sequence identity, predicted to react with Rat
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.
It 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 that forms homodimers or heterodimers 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 (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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