Rat IFN-γ Recombinant Rabbit mAb (S-3603) Size:100μg Autosomal recessive mutations in the

Autosomal recessive mutations in the LOXL3 gene are one of the causes of Stickler syndrome

CXXC5 functions as a transcription factor in the cell nucleus and is involved in myelopoiesis

Tissue sampling and transportation is the first and most easily neglected link in the successful construction of organoids

Detection Range: 9

tissue (TGM2) capture antibody

Rat IFN-γ Recombinant Rabbit mAb (S-3603) Size:100μg Autosomal recessive mutations in theProduct Specification Host Rabbit Antigen IFN Clone Number S 3603 Antibody Type Recombinant mAb Isotype IgG Application ELISA Reactivity Rt Purification Protein A Concentration 0. 5 mg ml Conjugation Unconjugated Physical Appearance Liquid Storage Buffer PBS, 40% Glycerol, 0. 05% BSA, 0. 03% Proclin 300 Stability & Storage 12 months from date of receipt reconstitution, 20 C as supplied Dilution application dilution species ELISA 1: 5000 1: 10000 Rt