donkey anti rabbit igg fitc Search Results


fitc  (Bioss)
93
Bioss fitc
Fitc, supplied by Bioss, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Bio-Rad donkey anti rabbit igg fitc
Donkey Anti Rabbit Igg Fitc, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Jackson Immuno affinipure donkey anti rabbit igg
Affinipure Donkey Anti Rabbit Igg, supplied by Jackson Immuno, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Jackson Immuno fluorescein conjugated donkey anti rabbit igg
Fluorescein Conjugated Donkey Anti Rabbit Igg, supplied by Jackson Immuno, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Santa Cruz Biotechnology fitc
Fitc, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Rockland Immunochemicals fluorescein isothiocyanate conjugated donkey anti rabbit igg
Fluorescein Isothiocyanate Conjugated Donkey Anti Rabbit Igg, supplied by Rockland Immunochemicals, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Jackson Immuno fluorescein fitc donkey anti rabbit igg
KEY RESOURCES TABLE
Fluorescein Fitc Donkey Anti Rabbit Igg, supplied by Jackson Immuno, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Biorbyt fitc conjugated donkey anti rabbit igg
KEY RESOURCES TABLE
Fitc Conjugated Donkey Anti Rabbit Igg, supplied by Biorbyt, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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SeraCare Life Sciences fitc-conjugated donkey anti-rabbit igg antibody cat. no. 02–18-06
KEY RESOURCES TABLE
Fitc Conjugated Donkey Anti Rabbit Igg Antibody Cat. No. 02–18 06, supplied by SeraCare Life Sciences, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Biozol Diagnostica Vertrieb GmbH fitc- or cy™5-conjugated polyclonal donkey anti–rabbit igg
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 <t>(goat</t> <t>polyclonal),</t> 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 <t>FITC-labeled</t> 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.
Fitc Or Cy™5 Conjugated Polyclonal Donkey Anti–Rabbit Igg, supplied by Biozol Diagnostica Vertrieb GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Immunotec inc donkey anti-rabbit igg conjugated to fluoresceine isothiocyanate (fitc)
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 <t>(goat</t> <t>polyclonal),</t> 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 <t>FITC-labeled</t> 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.
Donkey Anti Rabbit Igg Conjugated To Fluoresceine Isothiocyanate (Fitc), supplied by Immunotec inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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MBL Life science secondary donkey anti-rabbit igg (h+l chain) polyclonal antibody fitc
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 <t>(goat</t> <t>polyclonal),</t> 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 <t>FITC-labeled</t> 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.
Secondary Donkey Anti Rabbit Igg (H+L Chain) Polyclonal Antibody Fitc, supplied by MBL Life science, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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Image Search Results


KEY RESOURCES TABLE

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: Fluorescein (FITC)-Donkey Anti-Rabbit IgG , Jackson ImmunoResearch Labs , Cat# 711-097-003; RRID:AB_2340598.

Techniques: Virus, Recombinant, Tube Formation Assay, In Vivo, Angiogenesis Assay, Enzyme-linked Immunosorbent Assay, Lactate Assay, Plasmid Preparation, Software

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.

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: FITC- or Cy™5-conjugated polyclonal goat anti–mouse IgM (μH chain specific) and FITC- or Cy™5-conjugated polyclonal donkey anti–rabbit IgG (Dianova); FITC-conjugated anti–κL-chain and anti–λ 1 +λ 2 L-chain mAbs (BD Biosciences); polyclonal rabbit anti-TdT (Supertechs); and polyclonal rabbit anti-Ku70 (DPC Biermann).

Techniques: Isolation, Staining, Amplification, Flow Cytometry, Labeling