rabbit anti-mouse igg2b Search Results


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Fig. 3. APP staining to show the temporal and spatial analysis of axonal damage after focal cerebral ischemia. Accumulation of amyloid precursor protein (APP) was monitored with a rabbit <t>polyclonal</t> anti-APP antibody ( red ) and compared with staining for normal myelin using a mouse monoclonal anti-MBP ( green ). ( a – c ) Representative confocal images of sections double labeled for MBP and APP in the core of the infarct ( left ). The center is out of view to the left. In the merged images from the edge of the infarct ( right ), arrowheads surround a myelinated bundle containing puncta of APP staining. Scale bars = 100 µ m (adapted with permission and modifi cation from ref. 1 ).
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Fig. 3. APP staining to show the temporal and spatial analysis of axonal damage after focal cerebral ischemia. Accumulation of amyloid precursor protein (APP) was monitored with a rabbit <t>polyclonal</t> anti-APP antibody ( red ) and compared with staining for normal myelin using a mouse monoclonal anti-MBP ( green ). ( a – c ) Representative confocal images of sections double labeled for MBP and APP in the core of the infarct ( left ). The center is out of view to the left. In the merged images from the edge of the infarct ( right ), arrowheads surround a myelinated bundle containing puncta of APP staining. Scale bars = 100 µ m (adapted with permission and modifi cation from ref. 1 ).
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Fig. 3. APP staining to show the temporal and spatial analysis of axonal damage after focal cerebral ischemia. Accumulation of amyloid precursor protein (APP) was monitored with a rabbit <t>polyclonal</t> anti-APP antibody ( red ) and compared with staining for normal myelin using a mouse monoclonal anti-MBP ( green ). ( a – c ) Representative confocal images of sections double labeled for MBP and APP in the core of the infarct ( left ). The center is out of view to the left. In the merged images from the edge of the infarct ( right ), arrowheads surround a myelinated bundle containing puncta of APP staining. Scale bars = 100 µ m (adapted with permission and modifi cation from ref. 1 ).
Rabbit Anti Mouse Igg2b, supplied by Novus Biologicals, 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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Fig. 3. APP staining to show the temporal and spatial analysis of axonal damage after focal cerebral ischemia. Accumulation of amyloid precursor protein (APP) was monitored with a rabbit <t>polyclonal</t> anti-APP antibody ( red ) and compared with staining for normal myelin using a mouse monoclonal anti-MBP ( green ). ( a – c ) Representative confocal images of sections double labeled for MBP and APP in the core of the infarct ( left ). The center is out of view to the left. In the merged images from the edge of the infarct ( right ), arrowheads surround a myelinated bundle containing puncta of APP staining. Scale bars = 100 µ m (adapted with permission and modifi cation from ref. 1 ).
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Fig. 3. APP staining to show the temporal and spatial analysis of axonal damage after focal cerebral ischemia. Accumulation of amyloid precursor protein (APP) was monitored with a rabbit <t>polyclonal</t> anti-APP antibody ( red ) and compared with staining for normal myelin using a mouse monoclonal anti-MBP ( green ). ( a – c ) Representative confocal images of sections double labeled for MBP and APP in the core of the infarct ( left ). The center is out of view to the left. In the merged images from the edge of the infarct ( right ), arrowheads surround a myelinated bundle containing puncta of APP staining. Scale bars = 100 µ m (adapted with permission and modifi cation from ref. 1 ).
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Fig. 3. APP staining to show the temporal and spatial analysis of axonal damage after focal cerebral ischemia. Accumulation of amyloid precursor protein (APP) was monitored with a rabbit <t>polyclonal</t> anti-APP antibody ( red ) and compared with staining for normal myelin using a mouse monoclonal anti-MBP ( green ). ( a – c ) Representative confocal images of sections double labeled for MBP and APP in the core of the infarct ( left ). The center is out of view to the left. In the merged images from the edge of the infarct ( right ), arrowheads surround a myelinated bundle containing puncta of APP staining. Scale bars = 100 µ m (adapted with permission and modifi cation from ref. 1 ).
Rabbit Igg Conjugated To Irdye 680, supplied by Rockland Immunochemicals, used in various techniques. Bioz Stars score: 88/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Fig. 3. APP staining to show the temporal and spatial analysis of axonal damage after focal cerebral ischemia. Accumulation of amyloid precursor protein (APP) was monitored with a rabbit <t>polyclonal</t> anti-APP antibody ( red ) and compared with staining for normal myelin using a mouse monoclonal anti-MBP ( green ). ( a – c ) Representative confocal images of sections double labeled for MBP and APP in the core of the infarct ( left ). The center is out of view to the left. In the merged images from the edge of the infarct ( right ), arrowheads surround a myelinated bundle containing puncta of APP staining. Scale bars = 100 µ m (adapted with permission and modifi cation from ref. 1 ).
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Rockland Immunochemicals dylight 549 conjugated anti mouse igg
Fig. 3. APP staining to show the temporal and spatial analysis of axonal damage after focal cerebral ischemia. Accumulation of amyloid precursor protein (APP) was monitored with a rabbit <t>polyclonal</t> anti-APP antibody ( red ) and compared with staining for normal myelin using a mouse monoclonal anti-MBP ( green ). ( a – c ) Representative confocal images of sections double labeled for MBP and APP in the core of the infarct ( left ). The center is out of view to the left. In the merged images from the edge of the infarct ( right ), arrowheads surround a myelinated bundle containing puncta of APP staining. Scale bars = 100 µ m (adapted with permission and modifi cation from ref. 1 ).
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Rockland Immunochemicals rabbit anti mouse igg dylight 488 conjugated antibody
Fig. 3. APP staining to show the temporal and spatial analysis of axonal damage after focal cerebral ischemia. Accumulation of amyloid precursor protein (APP) was monitored with a rabbit <t>polyclonal</t> anti-APP antibody ( red ) and compared with staining for normal myelin using a mouse monoclonal anti-MBP ( green ). ( a – c ) Representative confocal images of sections double labeled for MBP and APP in the core of the infarct ( left ). The center is out of view to the left. In the merged images from the edge of the infarct ( right ), arrowheads surround a myelinated bundle containing puncta of APP staining. Scale bars = 100 µ m (adapted with permission and modifi cation from ref. 1 ).
Rabbit Anti Mouse Igg Dylight 488 Conjugated Antibody, supplied by Rockland Immunochemicals, 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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Cedarlane lysis anti cd8 igm mab ascites clone 3 155 and rabbit complement cedarlane
Fig. 3. APP staining to show the temporal and spatial analysis of axonal damage after focal cerebral ischemia. Accumulation of amyloid precursor protein (APP) was monitored with a rabbit <t>polyclonal</t> anti-APP antibody ( red ) and compared with staining for normal myelin using a mouse monoclonal anti-MBP ( green ). ( a – c ) Representative confocal images of sections double labeled for MBP and APP in the core of the infarct ( left ). The center is out of view to the left. In the merged images from the edge of the infarct ( right ), arrowheads surround a myelinated bundle containing puncta of APP staining. Scale bars = 100 µ m (adapted with permission and modifi cation from ref. 1 ).
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Image Search Results


Fig. 3. APP staining to show the temporal and spatial analysis of axonal damage after focal cerebral ischemia. Accumulation of amyloid precursor protein (APP) was monitored with a rabbit polyclonal anti-APP antibody ( red ) and compared with staining for normal myelin using a mouse monoclonal anti-MBP ( green ). ( a – c ) Representative confocal images of sections double labeled for MBP and APP in the core of the infarct ( left ). The center is out of view to the left. In the merged images from the edge of the infarct ( right ), arrowheads surround a myelinated bundle containing puncta of APP staining. Scale bars = 100 µ m (adapted with permission and modifi cation from ref. 1 ).

Journal: Springer Protocols Handbooks

Article Title: Animal Models of Acute Neurological Injuries II

doi: 10.1007/978-1-61779-782-8

Figure Lengend Snippet: Fig. 3. APP staining to show the temporal and spatial analysis of axonal damage after focal cerebral ischemia. Accumulation of amyloid precursor protein (APP) was monitored with a rabbit polyclonal anti-APP antibody ( red ) and compared with staining for normal myelin using a mouse monoclonal anti-MBP ( green ). ( a – c ) Representative confocal images of sections double labeled for MBP and APP in the core of the infarct ( left ). The center is out of view to the left. In the merged images from the edge of the infarct ( right ), arrowheads surround a myelinated bundle containing puncta of APP staining. Scale bars = 100 µ m (adapted with permission and modifi cation from ref. 1 ).

Article Snippet: 1° Antibodies—same as for Western blot protocol: (a) 4-HNE: Monoclonal antibody (JaICA, Cat# MHN-020P). (b) Acrolein: Rabbit polyclonal anti-acrolein (Novus Biologicals Inc., Cat# NB200-556). (c) 3-NT: Nitrotyrosine Mouse IgG2b IgG monoclonal Antibody (GenWay Biotech, Inc. Cat#: 20-321- 175259). (d) Protein carbonyl: Rabbit α -DNP antibody (Chemicon international, Cat: 90451, Chemicon International Oxyblot ® Protein Oxidation Detection Kit S7150 or Sigma Rabbit α -DNP antibody: D9656).

Techniques: Staining, Labeling