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ROBO3, Polyclonal Antibody

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產(chǎn)品名稱: ROBO3, Polyclonal Antibody
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ROBO3, Polyclonal Antibody


ROBO3, Polyclonal Antibody  的詳細(xì)介紹
Product Name

ROBO3, Polyclonal Antibody

Full Product Name

ROBO3 Antibody - C-terminal region

Product Gene Name

anti-ROBO3 antibody

[Similar Products]
Product Synonym Gene Name
ROBO3;[Similar Products]
Antibody/Peptide Pairs
ROBO3 peptide (MBS3244443) is used for blocking the activity of ROBO3 antibody (MBS3219569)
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
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Immunogen Sequence
Synthetic peptide located within the following region: HPSRSPSAQE PRGSCCPSNP DPDDRYYNEA GISLYLAQTA RGTAAPGEGP
OMIM
607313
3D Structure
ModBase 3D Structure for Q96MS0
Clonality
Polyclonal
Host
Rabbit
Species Reactivity
Human
Purity/Purification
Affinity Purified
Form/Format
Liquid. Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
Immunogen
The immunogen is a synthetic peptide directed towards the C-terminal region of Human ROBO3
Preparation and Storage
For short term use, store at 2-8 degree C up to 1 week. For long term storage, store at -20 degree C in small aliquots to prevent freeze-thaw cycles.
Other Notes
Small volumes of anti-ROBO3 antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
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Related Product Information for
anti-ROBO3 antibody
This is a rabbit polyclonal antibody against ROBO3. It was validated on Western Blot

Target Description: This gene is a member of the Roundabout (ROBO) gene family that controls neurite outgrowth, growth cone guidance, and axon fasciculation. ROBO proteins are a subfamily of the immunoglobulin transmembrane receptor superfamily. SLIT proteins 1-3, a family of secreted chemorepellants, are ligands for ROBO proteins and SLIT/ROBO interactions regulate myogenesis, leukocyte migration, kidney morphogenesis, angiogenesis, and vasculogenesis in addition to neurogenesis. This gene, ROBO3, has a putative extracellular domain with five immunoglobulin (Ig)-like loops and three fibronectin (Fn) type III motifs, a transmembrane segment, and a cytoplasmic tail with three conserved signaling motifs: CC0, CC2, and CC3 (CC for conserved cytoplasmic). Unlike other ROBO family members, ROBO3 lacks motif CC1. The ROBO3 gene regulates axonal navigation at the ventral midline of the neural tube. In mouse, loss of Robo3 results in a complete failure of commissural axons to cross the midline throughout the spinal cord and the hindbrain. Mutations ROBO3 result in horizontal gaze palsy with progressive scoliosis (HGPPS); an autosomal recessive disorder characterized by congenital absence of horizontal gaze, progressive scoliosis, and failure of the corticospinal and somatosensory axon tracts to cross the midline in the medulla. Alternative transcript variants have been described but have not been experimentally validated.
Product Categories/Family for anti-ROBO3 antibody
Polyclonal; Neurobiology; Membrane Protein; Immunology; Disease Related; Meiosis/Mitosis/Cell Cycle;
Applications Tested/Suitable for anti-ROBO3 antibody
Western Blot (WB)

Western Blot (WB) of anti-ROBO3 antibody
Host: Rabbit
Target Name: ROBO3
Sample Type: 721_B Whole Cell lysates
Antibody Dilution: 1ug/ml
anti-ROBO3 antibody Western Blot (WB) (WB) image
Western Blot (WB) of anti-ROBO3 antibody
Host: Rabbit
Target Name: ROBO3
Sample Type: Jurkat Whole Cell lysates
Antibody Dilution: 1.0ug/ml
anti-ROBO3 antibody Western Blot (WB) (WB) image
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NCBI/Uniprot data below describe general gene information for ROBO3. It may not necessarily be applicable to this product.
NCBI GI #
48476182
NCBI GeneID
64221
NCBI Accession #
NP_071765 [Other Products]
NCBI GenBank Nucleotide #
NM_022370.4 [Other Products]
UniProt Primary Accession #
Q96MS0 [Other Products]
UniProt Related Accession #
Q96MS0[Other Products]
Molecular Weight
152kDa
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NCBI Official Full Name
roundabout homolog 3
NCBI Official Synonym Full Names
roundabout guidance receptor 3
NCBI Official Symbol
ROBO3??[Similar Products]
NCBI Official Synonym Symbols
HGPS; RIG1; HGPPS; RBIG1; HGPPS1
??[Similar Products]
NCBI Protein Information
roundabout homolog 3
UniProt Protein Name
Roundabout homolog 3
UniProt Synonym Protein Names
Roundabout-like protein 3
Protein Family
Roundabout
UniProt Gene Name
ROBO3??[Similar Products]
UniProt Entry Name
ROBO3_HUMAN
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NCBI Summary for ROBO3
This gene is a member of the Roundabout (ROBO) gene family that controls neurite outgrowth, growth cone guidance, and axon fasciculation. ROBO proteins are a subfamily of the immunoglobulin transmembrane receptor superfamily. SLIT proteins 1-3, a family of secreted chemorepellants, are ligands for ROBO proteins and SLIT/ROBO interactions regulate myogenesis, leukocyte migration, kidney morphogenesis, angiogenesis, and vasculogenesis in addition to neurogenesis. This gene, ROBO3, has a putative extracellular domain with five immunoglobulin (Ig)-like loops and three fibronectin (Fn) type III motifs, a transmembrane segment, and a cytoplasmic tail with three conserved signaling motifs: CC0, CC2, and CC3 (CC for conserved cytoplasmic). Unlike other ROBO family members, ROBO3 lacks motif CC1. The ROBO3 gene regulates axonal navigation at the ventral midline of the neural tube. In mouse, loss of Robo3 results in a complete failure of commissural axons to cross the midline throughout the spinal cord and the hindbrain. Mutations ROBO3 result in horizontal gaze palsy with progressive scoliosis (HGPPS); an autosomal recessive disorder characterized by congenital absence of horizontal gaze, progressive scoliosis, and failure of the corticospinal and somatosensory axon tracts to cross the midline in the medulla. Alternative transcript variants have been described but have not been experimentally validated. [provided by RefSeq, Dec 2009]
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Research Articles on ROBO3
1. T) causing a premature stop codon which is a disease-making mutation.">In our case, we found a novel homozygous mutation p.R842* (c.2524C>T) causing a premature stop codon which is a disease-making mutation.
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Precautions
All of MyBioSource's Products are for scientific laboratory research purposes and are not for diagnostic, therapeutics, prophylactic or in vivo use. Through your purchase, you expressly represent and warrant to MyBioSource that you will properly test and use any Products purchased from MyBioSource in accordance with industry standards. MyBioSource and its authorized distributors reserve the right to refuse to process any order where we reasonably believe that the intended use will fall outside of our acceptable guidelines.
Disclaimer
While every efforts were made to ensure the accuracy of the information provided in this datasheet, MyBioSource will not be liable for any omissions or errors contained herein. MyBioSource reserves the right to make changes to this datasheet at any time without prior notice.

It is the responsibility of the customer to report product performance issues to MyBioSource within 30 days of receipt of the product. Please visit our Terms & Conditions page for more information.
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