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map2 neuromics ch22103 chicken polyclonal icc  (Neuromics)


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    Neuromics map2 neuromics ch22103 chicken polyclonal icc
    Fig. 3. Specific immunostaining of hGCase in H4 cells and human neurons with hGCase-1/23 and hGCase-1/17. A) GBA1 + /+ and GBA1–/– H4 cells were fixed with 4% PFA, permeabilized with 0.05% Saponin, and stained with hGCase-1/23 and hGCase-1/17, together with a LAMP1 antibody. Scale bars: 10 m, and 1.5 m in inserts. (B) GBA1 + /+ and GBA1–/– human neurons were stained with hGCase-1/23, together with LAMP1 and <t>MAP2</t> antibodies. Scale bars: 100 m, and 25 m in inserts.
    Map2 Neuromics Ch22103 Chicken Polyclonal Icc, supplied by Neuromics, used in various techniques. Bioz Stars score: 93/100, based on 47 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/map2+neuromics+ch22103+chicken/MAP2+(Microtubule+assoc%2E+protein+2)/10__3233_slash_jpd___230295-78-91-92
    Average 93 stars, based on 47 article reviews
    map2 neuromics ch22103 chicken polyclonal icc - by Bioz Stars, 2026-09
    93/100 stars

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    1) Product Images from "Characterization of Novel Human β-glucocerebrosidase Antibodies for Parkinson’s Disease Research"

    Article Title: Characterization of Novel Human β-glucocerebrosidase Antibodies for Parkinson’s Disease Research

    Journal: Journal of Parkinson's Disease

    doi: 10.3233/jpd-230295

    Fig. 3. Specific immunostaining of hGCase in H4 cells and human neurons with hGCase-1/23 and hGCase-1/17. A) GBA1 + /+ and GBA1–/– H4 cells were fixed with 4% PFA, permeabilized with 0.05% Saponin, and stained with hGCase-1/23 and hGCase-1/17, together with a LAMP1 antibody. Scale bars: 10 m, and 1.5 m in inserts. (B) GBA1 + /+ and GBA1–/– human neurons were stained with hGCase-1/23, together with LAMP1 and MAP2 antibodies. Scale bars: 100 m, and 25 m in inserts.
    Figure Legend Snippet: Fig. 3. Specific immunostaining of hGCase in H4 cells and human neurons with hGCase-1/23 and hGCase-1/17. A) GBA1 + /+ and GBA1–/– H4 cells were fixed with 4% PFA, permeabilized with 0.05% Saponin, and stained with hGCase-1/23 and hGCase-1/17, together with a LAMP1 antibody. Scale bars: 10 m, and 1.5 m in inserts. (B) GBA1 + /+ and GBA1–/– human neurons were stained with hGCase-1/23, together with LAMP1 and MAP2 antibodies. Scale bars: 100 m, and 25 m in inserts.

    Techniques Used: Immunostaining, Staining

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    Fig. 3. Specific immunostaining of hGCase in H4 cells and human neurons with hGCase-1/23 and hGCase-1/17. A) GBA1 + /+ and GBA1–/– H4 cells were fixed with 4% PFA, permeabilized with 0.05% Saponin, and stained with hGCase-1/23 and hGCase-1/17, together with a LAMP1 antibody. Scale bars: 10 m, and 1.5 m in inserts. (B) GBA1 + /+ and GBA1–/– human neurons were stained with hGCase-1/23, together with LAMP1 and <t>MAP2</t> antibodies. Scale bars: 100 m, and 25 m in inserts.
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    Fig. 3. Specific immunostaining of hGCase in H4 cells and human neurons with hGCase-1/23 and hGCase-1/17. A) GBA1 + /+ and GBA1–/– H4 cells were fixed with 4% PFA, permeabilized with 0.05% Saponin, and stained with hGCase-1/23 and hGCase-1/17, together with a LAMP1 antibody. Scale bars: 10 m, and 1.5 m in inserts. (B) GBA1 + /+ and GBA1–/– human neurons were stained with hGCase-1/23, together with LAMP1 and <t>MAP2</t> antibodies. Scale bars: 100 m, and 25 m in inserts.
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    Fig. 3. Specific immunostaining of hGCase in H4 cells and human neurons with hGCase-1/23 and hGCase-1/17. A) GBA1 + /+ and GBA1–/– H4 cells were fixed with 4% PFA, permeabilized with 0.05% Saponin, and stained with hGCase-1/23 and hGCase-1/17, together with a LAMP1 antibody. Scale bars: 10 m, and 1.5 m in inserts. (B) GBA1 + /+ and GBA1–/– human neurons were stained with hGCase-1/23, together with LAMP1 and <t>MAP2</t> antibodies. Scale bars: 100 m, and 25 m in inserts.
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    Fig. 3. Specific immunostaining of hGCase in H4 cells and human neurons with hGCase-1/23 and hGCase-1/17. A) GBA1 + /+ and GBA1–/– H4 cells were fixed with 4% PFA, permeabilized with 0.05% Saponin, and stained with hGCase-1/23 and hGCase-1/17, together with a LAMP1 antibody. Scale bars: 10 m, and 1.5 m in inserts. (B) GBA1 + /+ and GBA1–/– human neurons were stained with hGCase-1/23, together with LAMP1 and MAP2 antibodies. Scale bars: 100 m, and 25 m in inserts.

    Journal: Journal of Parkinson's Disease

    Article Title: Characterization of Novel Human β-glucocerebrosidase Antibodies for Parkinson’s Disease Research

    doi: 10.3233/jpd-230295

    Figure Lengend Snippet: Fig. 3. Specific immunostaining of hGCase in H4 cells and human neurons with hGCase-1/23 and hGCase-1/17. A) GBA1 + /+ and GBA1–/– H4 cells were fixed with 4% PFA, permeabilized with 0.05% Saponin, and stained with hGCase-1/23 and hGCase-1/17, together with a LAMP1 antibody. Scale bars: 10 m, and 1.5 m in inserts. (B) GBA1 + /+ and GBA1–/– human neurons were stained with hGCase-1/23, together with LAMP1 and MAP2 antibodies. Scale bars: 100 m, and 25 m in inserts.

    Article Snippet: Antibody Source Catalog # Host Clonality Assays hGCase-1/17 Roche & NHGRI Available through MJFF soon Mouse Monoclonal ICC: 10 – 25 g mL hGCase-1/23 Roche & NHGRI Available through MJFF soon Mouse Monoclonal ICC: 10 – 25 g mL 812201 R&D systems MAB7410 Mouse Monoclonal Capillary WB 1 : 50 2E2 Abnova H00002629-M01 Mouse Monoclonal Conventional WB: 1 : 1000 Capillary WB: 1 : 50 EPR5143 Abcam ab128879 Rabbit Monoclonal Conventional WB: 1 : 1000 Capillary WB: 1 : 50 LAMP1 Cell Signaling Tech D2D11 Rabbit Monoclonal ICC: 1 : 400 MAP2 Neuromics CH22103 Chicken Polyclonal ICC: 1 : 400 LIMP2 Abcam ab176317 Rabbit Monoclonal Conventional WB: 1 : 1000 Western blot: Conventional chemiluminescence platform For each sample, 40 g of protein was loaded onto a 4–20% Mini-PROTEAN TGX PVDF gel (Bio-Rad Laboratories).

    Techniques: Immunostaining, Staining