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Thermo Fisher Scientific ROBO3 Polyclonal Antibody, MaxPab
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Thermo Fisher Scientific ROBO3 Polyclonal Antibody, MaxPab

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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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마지막 업데이트 2025. 08. 05. 오전 10:09
Thermo Fisher Scientific H00064221-B02P ROBO3 Polyclonal Antibody, MaxPab 50 ug pk판매 단위 pk ·
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518,100원VAT 포함 569,910원

Thermo Fisher Scientific · Thermo Fisher Scientific ROBO3 Polyclonal Antibody, MaxPab

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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