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beta-amyloid 29-40

" in TargetMol Product Catalog
  • Inhibitors & Agonists
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β-Amyloid (29-40)
TP1231184865-04-1
β-Amyloid (29-40) is a fragment of Amyloid-β peptide. Alzheimer's beta amyloid peptide (29-40 42) C-terminal fragments exhibit physical and chemical properties similar to fusion peptides of viral proteins, inducing liposome fusion in vitro.
  • $63
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[Arg6]-β-Amyloid (1-40), england mutation
T835091802084-26-9
β-Amyloid (1-40), England mutation, is a biologically active peptide with a histidine (His) to arginine (Arg) substitution at position 6, known to enhance oligomerization kinetics that serve as fibril seeds and increase neurotoxicity in cultured neurons. This alteration is one of several mutations in the beta-amyloid precursor gene implicated in autosomal dominant Alzheimer's Disease across multiple kindreds.
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(Gln22,Asn23)-Amyloid β-Protein (1-40)
T83541374796-75-5
(Gln22,Asn23)-Amyloid β-Protein (1-40) is a peptide used to study Cerebral Amyloid Angiopathy Mutations [1].
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β-Amyloid (1-40) (rat)
TP1441144409-98-3
Rat form of the beta-Amyloid (1-40) peptide
  • $162
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(Pyr11)-Amyloid β-Protein (11-40)
T83539192377-94-9
(Pyr11)-Amyloid β-Protein (11-40) (Aβ11pE-40), a peptide, is utilized in Alzheimer's disease research [1].
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β-Amyloid (1-40) (TFA)
T75751
β-Amyloid (1-40) TFA, a principal protein in plaques observed in the brains of Alzheimer's disease patients [1], is pivotal in research focused on this neurodegenerative disorder.
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β-Amyloid (1-40), FAM-labeled
T391461678416-08-4
β-Amyloid (1-40), FAM-labeled, is a β-Amyloid (1-40) peptide tagged with a FAM fluorescent label, exhibiting an excitation wavelength (λ ex) of 492 nm and an emission wavelength (λ em) of 518 nm.
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Beta-Amyloid(1-14),mouse,rat
TP1733
Beta-Amyloid(1-14),mouse,rat is a 1 to 14 fragment of Amyloid-β peptide. This peptide is amino acids 1 to 14 fragment of Beta-Amyloid peptide.
  • $63
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β-Amyloid (1-40), FAM-labeled TFA
T76086
β-Amyloid (1-40), FAM-labeled TFA, is a FAM fluorescently-labeled β-Amyloid (1-40) peptide (λ ex = 492 nm and λ em = 518 nm) [1].
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β-Amyloid (33-40)
TP1719634204-57-2
β-Amyloid (33-40) is a peptide composed of amino acids 33 to 40 from the beta-amyloid protein.
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(Gly22)-amyloid beta-protein(1-40)
T83540175010-18-1
Amyloid beta-protein(1-40) Arctic variant (Ab40ARC (E22G)), featuring a glycine at position 22 (Gly22), is a peptide utilized in Alzheimer's disease research [1].
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Biotin-β-Amyloid (1-40)
T39285183906-14-1
Biotin-β-Amyloid (1-40) is an amyloid-β-(1-40) peptide with an N-terminal biotinylation.
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β-Amyloid (1-40)
TP1303131438-79-4
Amyloid β1-40 is one of the fragments generated after cleavage of the amyloid peptide precursor protein by β and γ secretases.
  • $1,410
35 days
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β-Amyloid (22-40)
TP15441206779-25-0
This synthetic peptide consists of amino acids 22 to 40 of beta amyloid protein. This peptide sequence is often used in beta amyloid structure and aggregation studies.
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Biotin-β-Amyloid (17-40)
T76087
Biotin-β-Amyloid (17-40) is a biotinylated amyloid-ß-(1-40) peptide labeled at the N-terminal, comprising a 24-residue fragment from the post-translational processing of amyloid precursor protein (APP) [1].
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[Asn23]-beta-Amyloid (1-42), iowa mutation
T83506
[Asn23]-beta-Amyloid (1-42), Iowa mutation, is a biologically active peptide with increased aggregation propensity and fibril toxicity. This mutation involves the substitution of Aspartic acid (Asp) at position 23 with Asparagine (Asn), contributing to autosomal dominant Alzheimer's Disease and associated with severe cerebral amyloid beta-protein angiopathy (CAA) due to a missense alteration at position 694 of the amyloid precursor protein (APP) gene.
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[Asn23] β-Amyloid (1-40), Iowa mutation
T83507374796-72-2
[Asn23] β-Amyloid (1-40), Iowa mutation, is a biologically active peptide linked to autosomal dominant Alzheimer's Disease in multiple families. This involves the substitution of Asp 23 with Asn, causing severe cerebral amyloid beta-protein angiopathy (CAA). Individuals with this mutation exhibit a missense alteration in the APP gene at position 694, resulting in the mutated β-amyloid peptide aggregating more quickly and forming toxic fibrils.
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