Recombinant Anti-RET Vesicular Antibody, EV Displayed (VS-0425-YC312)
CAT#: VS-0425-YC312
The Recombinant Anti-RET Vesicular Antibody, EV Displayed (VS-0425-YC312) is an antibody-displaying extracellular vesicle (Ab-EV). The product combines the benefits of both extracellular vesicle (EV) and antibody (Ab) which can guide the decorated EVs to RET-expressed cells or tissues. The RET is a receptor tyrosine kinase important in neural development, with mutations associated with Hirschsprung disease and oncogenic activation.







Recombinant Antibody
- Application
- Cyt, ELISA, FC, Cell-uptake
- Product Type
- Ab-Fc-EVs
- Antibody Quantification (Ab/EV)
- ~100 Ab/EV
- Target
- RET
- Host Animal
- Human
- Antibody Isotype
- IgG
- Expression Cell
- Mammalian cell
Engineered EVs
- EV-sorting domain
- CD63
- Fc-binding domain
- z domain
- EV Size
- 30~150 nm
- Producing Cell
- HEK293F
- Isolation Method
- Gradient centrifugation
- Purification
- qEV size exclusion chromatography
- Binding Affinity
- Kd = 0.85 µg/mL
- Concentration
- 1 x 10¹⁰
- Size
- 1 mL
- Buffer
- PBS
- Storage
- Store at -80°C for 12 months
Target
- Full Name
- Ret proto-oncogene
- Biological Process
- Cell adhesion
- Molecular Function
- Kinase, Transferase, Tyrosine-protein kinase
- Cellular Localization
- Golgi apparatus, Cytosol, Plasma membrane
- Introduction
- This gene encodes a transmembrane receptor and member of the tyrosine protein kinase family of proteins. Binding of ligands such as GDNF (glial cell-line derived neurotrophic factor) and other related proteins to the encoded receptor stimulates receptor dimerization and activation of downstream signaling pathways that play a role in cell differentiation, growth, migration and survival. The encoded receptor is important in development of the nervous system, and the development of organs and tissues derived from the neural crest. This proto-oncogene can undergo oncogenic activation through both cytogenetic rearrangement and activating point mutations. Mutations in this gene are associated with Hirschsprung disease and central hypoventilation syndrome and have been identified in patients with renal agenesis. [provided by RefSeq, Sep 2017]
- Alternative Names
- CDHF12, CDHR16, HSCR1, MEN2A, MEN2B, MTC1, PTC, RET51
- Gene ID
- 5979
- UniProt ID
- P07949
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Related Diseases
Downloadable Resources
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Datasheet
MSDS
COA
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CAT | Product Name | Application | Type |
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CAT | Product Name | Application | Type |
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CAT | Product Name | Application | Type |
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CAT | Product Name | Application | Type |
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CAT | Product Name | Application | Type |
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CAT | Product Name | Application | Type |
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