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Santa Cruz Biotechnology
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Rockland Immunochemicals
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Jackson Immuno
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Biorbyt
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SeraCare Life Sciences
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Immunotec inc
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MBL Life science
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Image Search Results
Journal: Cell reports
Article Title: HIF-1α accumulation in response to transient hypoglycemia may worsen diabetic eye disease
doi: 10.1016/j.celrep.2022.111976
Figure Lengend Snippet: KEY RESOURCES TABLE
Article Snippet:
Techniques: Virus, Recombinant, Tube Formation Assay, In Vivo, Angiogenesis Assay, Enzyme-linked Immunosorbent Assay, Lactate Assay, Plasmid Preparation, Software
Journal: The Journal of Experimental Medicine
Article Title: Surface μ Heavy Chain Signals Down-Regulation of the V(D)J-Recombinase Machinery in the Absence of Surrogate Light Chain Components
doi: 10.1084/jem.20031523
Figure Lengend Snippet: μH chain is detectable on the surface of λ5 −/− , VpreB1 −/− VpreB2 −/− , and SLC −/− pre–B cells. (A) CD19 + BM cells were isolated by MACS from tet-μHC, tet-μHC λ5 −/− , and tet-μHC VpreB1 −/− VpreB2 −/− mice that had received Tet in drinking water for 7 d. Cells were expanded on stromal cells in medium containing IL-7 and Tet for 48 h, washed, and recultured for an additional 18 h in the presence of IL-7 with (shaded) or without Tet (unshaded). Cells were harvested and stained with biotinylated Abs against μH chain (goat polyclonal), pre-BCR (SL156), or SLC components (LM34, VP245, and R5). Surface-bound biotin was amplified and revealed by EAS and streptavidin-PE. Propidium iodide negative cells were analyzed by flow cytometry. (B) CD19 + BM cells were isolated by MACS from SLC −/− or Rag1 −/− (control) mice and expanded on stromal cells in medium containing IL-7 for 4 d. Cells were harvested and stained with FITC-labeled Abs against κ/λLC and biotinylated Abs against μHC (goat polyclonal) or λ5 (LM34). Surface-bound biotin was amplified and revealed aforementioned. Numbers represent the percentage of cells within the quadrants.
Article Snippet: For intracellular stainings, cells were fixed and permeabilized using the FIX & PERM ® kit (Caltag Laboratories) and the following antisera:
Techniques: Isolation, Staining, Amplification, Flow Cytometry, Labeling