
Thermo Fisher Scientific ROBO3 Polyclonal Antibody, MaxPab
ROBO3 단백질을 인식하는 Thermo Fisher Scientific의 폴리클로날 항체로, 인간 시료에 반응합니다. Western blot에 적합하며, PBS(pH 7.4) 용액 상태로 제공됩니다. 친화 크로마토그래피로 정제되었으며, -20°C에서 보관합니다. 연구용 전용 제품입니다.
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Applications
- Western Blot (WB): 1:500–1:1,000
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Mouse / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | ROBO3 (AAH08623.1, 1 a.a. ~147 a.a) full-length human protein |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | See Label |
| Purification | Affinity chromatography |
| Storage Buffer | PBS, pH 7.4 |
| Contains | No preservative |
| Storage Conditions | -20°C, Avoid Freeze/Thaw Cycles |
| Shipping Conditions | Ambient (domestic); Wet ice (international) |
Product Specific Information
Sequence of this protein is as follows:
MTPPLQGPRA RFRKKPKALP YRRENSPGDL PPPPLPPPEE EASWALELRA AGSMSSLERE RSGERKAVQA VPLAAQRVLH PDEEAWLPYS RPSFLSRGQG TSTCSTAGSN SSRGSSSSRG SRGPGRSRSQ SRSQSQRPGQ KRREEPR
Target Information
The ROBO3 gene belongs to the Roundabout (ROBO) family, which regulates neurite outgrowth, growth cone guidance, and axon fasciculation. ROBO proteins are part of the immunoglobulin transmembrane receptor superfamily. SLIT proteins (1–3) act as ligands for ROBO proteins, mediating processes such as myogenesis, leukocyte migration, kidney morphogenesis, angiogenesis, vasculogenesis, and neurogenesis.
ROBO3 has an extracellular domain with five Ig-like loops and three fibronectin type III motifs, a transmembrane region, and a cytoplasmic tail containing three conserved signaling motifs (CC0, CC2, CC3). Unlike other ROBO members, ROBO3 lacks the CC1 motif. It plays a crucial role in axonal navigation at the ventral midline of the neural tube. Loss of ROBO3 in mice leads to failure of commissural axons crossing the midline in the spinal cord and hindbrain. Mutations in ROBO3 are associated with horizontal gaze palsy with progressive scoliosis (HGPPS), an autosomal recessive disorder characterized by congenital absence of horizontal gaze and progressive scoliosis.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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