Protein L Protéines
(Protein L)
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Origine: Peptostreptococcus magnus
Hôte: Escherichia coli (E. coli)
Recombinant
>95 % as determined by SDS-PAGE.
1 reference
Origine: Peptostreptococcus magnus
Hôte: Escherichia coli (E. coli)
Recombinant
Origine: Others
Hôte: Escherichia coli (E. coli)
Recombinant
>98 % as determined by SDS-PAGE.
WB
Dernières publications pour nos Protein L Protéines
: "Impact of Site-Specific Conjugation of ScFv to Multifunctional Nanomedicines Using Second Generation Maleimide." dans: Bioconjugate chemistry, Vol. 29, Issue 5, pp. 1553-1559, (2019) (PubMed).: "A general platform for efficient extracellular expression and purification of Fab from Escherichia coli." dans: Applied microbiology and biotechnology, Vol. 103, Issue 8, pp. 3341-3353, (2019) (PubMed).
: "Magnetic nanocarriers for the specific delivery of siRNA: Contribution of breast cancer cells active targeting for down-regulation efficiency." dans: International journal of pharmaceutics, Vol. 569, pp. 118572, (2019) (PubMed).
: "Targeting HER2-breast tumors with scFv-decorated bimodal nanoprobes." dans: Journal of nanobiotechnology, Vol. 16, Issue 1, pp. 18, (2018) (PubMed).
: "Affinity chromatography on monolithic supports for simultaneous and high-throughput isolation of immunoglobulins from human serum." dans: Electrophoresis, Vol. 38, Issue 22-23, pp. 2909-2913, (2017) (PubMed).
: "Systemic treatment with CAR-engineered T cells against PSCA delays subcutaneous tumor growth and prolongs survival of mice." dans: BMC cancer, Vol. 14, pp. 30, (2014) (PubMed).
: "A novel chimeric antigen receptor against prostate stem cell antigen mediates tumor destruction in a humanized mouse model of pancreatic cancer." dans: Human gene therapy, Vol. 25, Issue 12, pp. 1003-12, (2014) (PubMed).
: "Redirected antitumor activity of primary human lymphocytes transduced with a fully human anti-mesothelin chimeric receptor." dans: Molecular therapy : the journal of the American Society of Gene Therapy, Vol. 20, Issue 3, pp. 633-43, (2012) (PubMed).
: "Recognition of glioma stem cells by genetically modified T cells targeting EGFRvIII and development of adoptive cell therapy for glioma." dans: Human gene therapy, Vol. 23, Issue 10, pp. 1043-53, (2012) (PubMed).
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