14 Results for "

Phage display

" in MedChemExpress (MCE) Product Catalog:
Products (14)

14 Results for "Phage display" in MCE Product Catalog:

Cat. No.: HY-125372
CAS No.: 16348-49-5
Purity:  99.85%
Synonyms: ABAO
Research Areas:  

Others

2-Amino benzamidoxime (ABAO) acts as a bioconjugation reagent precursor and a fluorescent probe precursor. 2-Amino benzamidoxime contains an aniline group for imine activation of aldehydes, as well as a nucleophilic group (Nu:) located at the ortho position of the amine, which is responsible for intramolecular cyclization. 2-Amino benzamidoxime reacts with glyoxal at the N-terminus of phage-displayed peptide libraries. Derivatives of 2-Amino benzamidoxime can be used for protein bioconjugation. Derivatives of 2-Amino benzamidoxime serve as fluorescent probes .\n



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Cat. No.: HY-P10424
CAS No.: 2378606-21-2
Target:  

PD-1/PD-L1

Research Areas:  

Cancer

OPBP-1 is a D-peptide obtained by phage display screening, molecular docking and molecular dynamics simulation. OPBP-1 has high stability and strong antitumor and oral activity. OPBP-1 can selectively bind PD-L1 protein, significantly block the interaction between PD-1 and PD-L1, and this blocking effect helps to restore and improve the function of T lymphocytes and reduce the proportion of bone marrow derived suppressor cells (MDSCs) to combat tumor-induced immune escape. OPBP-1 can be used in cancer immunotherapy research .
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Cat. No.: HY-P11422
Target:  

Peptides

Research Areas:  

Infection

CKS9 is an M cell-targeting polypeptide with the amino acid sequence CKSTHPLSC, forming a 9-mer peptide via cyclization through a disulfide bond between the two cysteine residues. CKS9 is obtained through phage display technology screening and has high affinity for M cells. CKS9 can promote chitosan nanoparticles to cross M cells and enter the follicle-associated epithelium (FAE) of intestinal Peyer's patches (PP). CKS9 can be used in studies related to swine dysentery and oral delivery .
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Cat. No.: HY-187404A
DOPE-PEG2000-CRPPR is an amphiphilic lipid-PEG-peptide conjugate consisting of DOPE (1,2-dioleoyl-sn-glycero-3-phosphoethanolamine), PEG2000, and the CRPPR peptide, a cardiac-targeting peptide identified by in vivo phage display. DOPE-PEG2000-CRPPR is used for heart-targeted drug delivery.
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Cat. No.: HY-187498A
DOPE-PEG2000-WLSEAGPVVTVRALRGTGSW is an amphiphilic lipid-PEG-peptide conjugate consisting of DOPE (1,2-dioleoyl-sn-glycero-3-phosphoethanolamine), PEG2000, and the WLSEAGPVVTVRALRGTGSW peptide, a 20-amino-acid targeting peptide identified through phage display. DOPE-PEG2000-WLSEAGPVVTVRALRGTGSW is used for targeted drug delivery via liposome and nanoparticle functionalization.
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Cat. No.: HY-187416A
Synonyms: DOPE-PEG2000-Mal-Cys-CGKRK
DOPE-PEG2000-CGKRK (DOPE-PEG2000-Mal-Cys-CGKRK) is an amphiphilic lipid-PEG-peptide conjugate consisting of DOPE (1,2-dioleoyl-sn-glycero-3-phosphoethanolamine), PEG2000, and the CGKRK peptide, a tumor-homing peptide identified by in vivo phage display. DOPE-PEG2000-CGKRK is used for tumor-targeted drug delivery through liposome and nanoparticle surface modification.
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Cat. No.: HY-187476A
Synonyms: DOPE-PEG2000-Mal-Cys-LTLRWVGLMS
DOPE-PEG2000-LTLRWVGLMS (DOPE-PEG2000-Mal-Cys-LTLRWVGLMS) is an amphiphilic lipid-PEG-peptide conjugate composed of DOPE (1,2-dioleoyl-sn-glycero-3-phosphoethanolamine), PEG2000, and the LTLRWVGLMS peptide, a tissue-targeting peptide identified through phage display. DOPE-PEG2000-LTLRWVGLMS is used for targeted drug delivery via liposome and nanoparticle functionalization.
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Cat. No.: HY-187490A
Synonyms: DOPE-PEG2000-Mal-Cys-CREKA
DOPE-PEG2000-CREKA (DOPE-PEG2000-Mal-Cys-CREKA) is an amphiphilic lipid-PEG-peptide conjugate consisting of DOPE (1,2-dioleoyl-sn-glycero-3-phosphoethanolamine), PEG2000, and the CREKA peptide (Cys-Arg-Glu-Lys-Ala), a tumor-homing peptide identified by in vivo phage display. DOPE-PEG2000-CREKA is used for tumor stroma-targeted drug delivery.
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Cat. No.: HY-187493A
Synonyms: DOPE-PEG2000-Mal-Cys-DHLASLWWGTEL
DOPE-PEG2000-DHLASLWWGTEL (DOPE-PEG2000-Mal-Cys-DHLASLWWGTEL) is an amphiphilic lipid-PEG-peptide conjugate composed of DOPE (1,2-dioleoyl-sn-glycero-3-phosphoethanolamine), PEG2000, and the DHLASLWWGTEL peptide, a 12-amino-acid tissue-targeting peptide identified through phage display. DOPE-PEG2000-DHLASLWWGTEL is used for targeted drug delivery through liposome and nanoparticle surface modification.
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Cat. No.: HY-P10739C
CAS No.: 1027630-05-2
Target:  

Collagen Apoptosis

Research Areas:  

Inflammation/Immunology

WYRGRLC is a type II collagen-targeting peptide. WYRGRLC specifically binds to type II collagen α1 in articular cartilage in a sequence-dependent manner. WYRGRLC inhibits the binding of WYRGRL-displaying phage (C1-3) to articular cartilage in a sequence-specific manner. WYRGRLC can act as a retention enhancer to improve the cartilage-targeting ability of polymeric nanoparticles and liposomal nanoplatforms, facilitating the delivery of Rapamycin (HY-10219) to chondrocytes. WYRGRLC can be used in studies related to osteoarthritis .
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Cat. No.: HY-187405A
Synonyms: DOPE-PEG2000-Mal-Cys-NYZL1
DOPE-PEG2000-NYZL1 (DOPE-PEG2000-Mal-Cys-NYZL1) is an amphiphilic lipid-PEG-peptide conjugate composed of DOPE (1,2-dioleoyl-sn-glycero-3-phosphoethanolamine), PEG2000, and the NYZL1 peptide, a tumor-targeting peptide identified through phage display. DOPE-PEG2000-NYZL1 is used for tumor-targeted drug delivery via liposome and nanoparticle functionalization.
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Cat. No.: HY-P11225
CAS No.: 2699627-67-1
Synonyms: MAP-04-02
Target:  

Bacterial

Research Areas:  

Infection

DRAMP18563 (MAP-04-02) is a linear antimicrobial peptide that can act as a delivery vector to transport dual-ring peptide inhibitors that cannot penetrate the outer membrane of Gram-negative bacteria to their target sites. DRAMP18563 can be used to study the delivery strategies of dual-ring peptide inhibitors .
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Cat. No.: HY-187415A
Synonyms: DOPE-PEG2000-Mal-Cys-TAASGVRSMH
DOPE-PEG2000-TAASGVRSMH is an amphiphilic lipid-PEG-peptide conjugate composed of 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (DOPE) , polyethylene glycol 2000 (PEG2000) , and the TAASGVRSMH peptide.
DOPE provides a hydrophobic phospholipid anchor for membrane insertion, PEG2000 forms a hydrophilic spacer that enhances circulation stability, and the TAASGVRSMH peptide serves as a tumor-vasculature-homing ligand identified by in vivo phage display.
This conjugate can be used to functionalize liposomes and lipid nanoparticles for targeted drug delivery to tumor vasculature.
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Cat. No.: HY-187474A
Synonyms: DOPE-PEG2000-Mal-Cys-HTMYYHHYQHHL
DOPE-PEG2000-K237 (DOPE-PEG2000-Mal-Cys-HTMYYHHYQHHL) is an amphiphilic lipid-PEG-peptide conjugate composed of DOPE (1,2-dioleoyl-sn-glycero-3-phosphoethanolamine), PEG2000, and the K237 peptide (sequence: HTMYYHHYQHHL). K237 peptide is a tumor-homing peptide identified by phage display that specifically binds to vasculature in tumor tissues. DOPE-PEG2000-K237 is used for tumor-targeted drug delivery via functionalization of liposomes and nanoparticles.
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