mouse ctx-i elisa kit Search Results


mouse cross linked c-telopeptide of type i collagen (ctxi) elisa kit  (Bioss)
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mouse ctx-i elisa kit  (AFG Bioscience LLC)
90
AFG Bioscience LLC mouse ctx-i elisa kit
( A ) Representative fluorescent TRAP staining images of femoral long bones from control and Csf1 CKO Adipoq mice at 3 months of age show TRAP+ osteoclasts at different skeletal sites: secondary spongiosa (SS), chondro-osseous junction (COJ), and endosteal surface (Endo.S). TB: trabecular bone; CB: cortical bone. Scale bar = 50 μm. ( B ) Quantification of osteoclast surface (Oc.S) at three skeletal sites. BS: bone surface. L: COJ length. n=5 mice/group. ***, p<0.001 CKO vs control. ( C ) Representative TRAP staining images of osteoclast culture derived from control and Csf1 CKO Adipoq BMMs at 7 days after addition of RANKL and Csf1. Arrows point to mature osteoclasts. Scale bar = 200 μm. ( D ) Quantification of TRAP+ multinucleated cells (>3 nuclei/cell) per field. n=7 mice/group. ( E ) Representative Osterix staining of trabecular bone from control and Csf1 CKO Adipoq femurs. Scale bar = 50 μm. ( F ) Quantification of osteoblast surface (OB.S). BS, bone surface. n=8–12 mice/group. ( G ) Representative double labeling of trabecular bone from control and Csf1 CKO Adipoq femurs. ( H ) Bone formation activity is quantified. MAR: mineral apposition rate; MS: mineralizing surface; BFR: bone formation rate. n=4 mice/group. ( I ) Serum <t>ELISA</t> analysis of bone resorption marker (CTX-1) and formation marker (PINP) in control and CKO mice. n=6–8 mice/group. *, p<0.05 CKO vs control. Figure 4—source data 1. Full dataset for . Figure 4—source data 2. Full dataset for . Figure 4—source data 3. Full dataset for . Figure 4—source data 4. Full dataset for . Figure 4—source data 5. Full dataset for .
Mouse Ctx I Elisa Kit, supplied by AFG Bioscience LLC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mouse+ctx-i+elisa+kit/mouse+ctx+i+elisa+kit/pmc10005765-220-17-21
Average 90 stars, based on 1 article reviews
mouse ctx-i elisa kit - by Bioz Stars, 2026-09
90/100 stars
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elisa kit ctxi mouse  (G Biosciences)
N/A
An ELISA kit for the detection of CTXI Mouse This uses Sandwich ELISA Double Antibody and has a sensitivity of 0 094ng ml
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Image Search Results


( A ) Representative fluorescent TRAP staining images of femoral long bones from control and Csf1 CKO Adipoq mice at 3 months of age show TRAP+ osteoclasts at different skeletal sites: secondary spongiosa (SS), chondro-osseous junction (COJ), and endosteal surface (Endo.S). TB: trabecular bone; CB: cortical bone. Scale bar = 50 μm. ( B ) Quantification of osteoclast surface (Oc.S) at three skeletal sites. BS: bone surface. L: COJ length. n=5 mice/group. ***, p<0.001 CKO vs control. ( C ) Representative TRAP staining images of osteoclast culture derived from control and Csf1 CKO Adipoq BMMs at 7 days after addition of RANKL and Csf1. Arrows point to mature osteoclasts. Scale bar = 200 μm. ( D ) Quantification of TRAP+ multinucleated cells (>3 nuclei/cell) per field. n=7 mice/group. ( E ) Representative Osterix staining of trabecular bone from control and Csf1 CKO Adipoq femurs. Scale bar = 50 μm. ( F ) Quantification of osteoblast surface (OB.S). BS, bone surface. n=8–12 mice/group. ( G ) Representative double labeling of trabecular bone from control and Csf1 CKO Adipoq femurs. ( H ) Bone formation activity is quantified. MAR: mineral apposition rate; MS: mineralizing surface; BFR: bone formation rate. n=4 mice/group. ( I ) Serum ELISA analysis of bone resorption marker (CTX-1) and formation marker (PINP) in control and CKO mice. n=6–8 mice/group. *, p<0.05 CKO vs control. Figure 4—source data 1. Full dataset for . Figure 4—source data 2. Full dataset for . Figure 4—source data 3. Full dataset for . Figure 4—source data 4. Full dataset for . Figure 4—source data 5. Full dataset for .

Journal: eLife

Article Title: Csf1 from marrow adipogenic precursors is required for osteoclast formation and hematopoiesis in bone

doi: 10.7554/eLife.82112

Figure Lengend Snippet: ( A ) Representative fluorescent TRAP staining images of femoral long bones from control and Csf1 CKO Adipoq mice at 3 months of age show TRAP+ osteoclasts at different skeletal sites: secondary spongiosa (SS), chondro-osseous junction (COJ), and endosteal surface (Endo.S). TB: trabecular bone; CB: cortical bone. Scale bar = 50 μm. ( B ) Quantification of osteoclast surface (Oc.S) at three skeletal sites. BS: bone surface. L: COJ length. n=5 mice/group. ***, p<0.001 CKO vs control. ( C ) Representative TRAP staining images of osteoclast culture derived from control and Csf1 CKO Adipoq BMMs at 7 days after addition of RANKL and Csf1. Arrows point to mature osteoclasts. Scale bar = 200 μm. ( D ) Quantification of TRAP+ multinucleated cells (>3 nuclei/cell) per field. n=7 mice/group. ( E ) Representative Osterix staining of trabecular bone from control and Csf1 CKO Adipoq femurs. Scale bar = 50 μm. ( F ) Quantification of osteoblast surface (OB.S). BS, bone surface. n=8–12 mice/group. ( G ) Representative double labeling of trabecular bone from control and Csf1 CKO Adipoq femurs. ( H ) Bone formation activity is quantified. MAR: mineral apposition rate; MS: mineralizing surface; BFR: bone formation rate. n=4 mice/group. ( I ) Serum ELISA analysis of bone resorption marker (CTX-1) and formation marker (PINP) in control and CKO mice. n=6–8 mice/group. *, p<0.05 CKO vs control. Figure 4—source data 1. Full dataset for . Figure 4—source data 2. Full dataset for . Figure 4—source data 3. Full dataset for . Figure 4—source data 4. Full dataset for . Figure 4—source data 5. Full dataset for .

Article Snippet: Sera were collected during mouse euthanization for measuring bone turnover markers, collagen type I C-telopeptide degradation products (mouse CTX-I ELISA Kit, AFG Scientific, Northbrook, IL, USA) and N-terminal propeptide of type I procollagen (Immunotag Mouse PINP ELISA Kit, G-Bioscience, St. Louis, MO, USA) respectively, according to the manufacturer’s instructions.

Techniques: Staining, Control, Derivative Assay, Labeling, Activity Assay, Enzyme-linked Immunosorbent Assay, Marker