Lirilumab Biosimilar – Anti-KIRD2 subgroup mAb – Research Grade

Reference:
Size

,

Isotype

Human IgG1

Brand

Product type

Clonality

Expression system

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Product nameLirilumab Biosimilar - Anti-KIRD2 subgroup mAb - Research Grade
SourceCAS 1000676-41-4
SpeciesHomo sapiens
Purity>85%
BufferPBS buffer PH7.5
Delivery conditionBlue ice (+4°C)
Delivery Time3-5 days if in stock; 3-5 weeks if production needed
Storage conditionstore at -80°C
BrandProteoGenix
Aliases /SynonymsLirilumab,BMS-986015,IPH2102,KIRD2 subgroup,anti-KIRD2 subgroup
ReferencePX-TA1297
NoteFor research use only. Not suitable for clinical or therapeutic use.
IsotypeHuman IgG1
ClonalityMonoclonal Antibody

Description of Lirilumab Biosimilar - Anti-KIRD2 subgroup mAb - Research Grade

General information on Anti-KIRD2 subgroup[Homo sapiens] (Lirilumab) Monoclonal Antibody

Lirilumab has been investigated for the treatment of Leukemia, Cancer, Multiple Myeloma, Lymphocytic Leukemia, and Acute Myeloid Leukemia.

SDS-PAGE for Lirilumab Biosimilar - Anti-KIRD2 subgroup mAb

Lirilumab Biosimilar - Anti-KIRD2 subgroup mAb, on SDS-PAGE under reducing and non-reducing condition. The gel was stained overnight with Coomassie Blue. The purity of the antibody is greater than 95%.

Lirilumab Biosimilar - Anti-KIRD2 subgroup mAb binds to CD158a / KIR2DL1, C-His, recombinant protein in indirect ELISA Assay

Immobilized CD158a / KIR2DL1, C-His, recombinant protein (cat. No.PX-P5573) at 0.5µg/mL (100µL/well) can bind to Lirilumab Biosimilar - Anti-KIRD2 subgroup mAb (cat. No.PX-TA1297) in indirect ELISA with Goat Anti-Human IgG secondary antibody coupled with HRP measured by OD450

Publication

  • Furkan Yigitbilek, Elif Ozdogan, Nitin Abrol, Walter D. Park, Michael J. Hansen, Surendra Dasari, Mark D. Stegall and Timucin Taner,Liver mesenchymal stem cells are superior inhibitors of NK cell functions through differences in their secretome compared to other mesenchymal stem cells,Front. Immunol., 21 September 2022, Sec. Alloimmunity and Transplantation, https://doi.org/10.3389/fimmu.2022.952262

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