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map1b  (Novus Biologicals)


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    Structured Review

    Novus Biologicals map1b
    IP of retinal lysate. The top panels show Western blot analysis of the <t>MAP1B</t> IP experimental samples probed with Tulp1 antibodies. In the IP product lane, a band corresponding to Tulp1 is detected. A corresponding band is seen in the rat retinal lysate and wt mouse retinal homogenate but not in the tulp1−/− retinal lysate, liver lysate or non-specific IgG IP lanes. The bottom panels show Western blot analysis of the MAP1B IP experimental samples probed with MAP1B antibodies. In the IP product, rat retinal lysate, wt mouse retinal lysate and tulp1−/− retinal lysate lanes, a band corresponding to MAP1B is detected. No bands are seen in the liver or non-specific IgG IP sample lanes.
    Map1b, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 91/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/map1b/product/Novus Biologicals
    Average 91 stars, based on 2 article reviews
    map1b - by Bioz Stars, 2026-02
    91/100 stars

    Images

    1) Product Images from "Photoreceptor Compartment-Specific TULP1 Interactomes"

    Article Title: Photoreceptor Compartment-Specific TULP1 Interactomes

    Journal: International Journal of Molecular Sciences

    doi: 10.3390/ijms22158066

    IP of retinal lysate. The top panels show Western blot analysis of the MAP1B IP experimental samples probed with Tulp1 antibodies. In the IP product lane, a band corresponding to Tulp1 is detected. A corresponding band is seen in the rat retinal lysate and wt mouse retinal homogenate but not in the tulp1−/− retinal lysate, liver lysate or non-specific IgG IP lanes. The bottom panels show Western blot analysis of the MAP1B IP experimental samples probed with MAP1B antibodies. In the IP product, rat retinal lysate, wt mouse retinal lysate and tulp1−/− retinal lysate lanes, a band corresponding to MAP1B is detected. No bands are seen in the liver or non-specific IgG IP sample lanes.
    Figure Legend Snippet: IP of retinal lysate. The top panels show Western blot analysis of the MAP1B IP experimental samples probed with Tulp1 antibodies. In the IP product lane, a band corresponding to Tulp1 is detected. A corresponding band is seen in the rat retinal lysate and wt mouse retinal homogenate but not in the tulp1−/− retinal lysate, liver lysate or non-specific IgG IP lanes. The bottom panels show Western blot analysis of the MAP1B IP experimental samples probed with MAP1B antibodies. In the IP product, rat retinal lysate, wt mouse retinal lysate and tulp1−/− retinal lysate lanes, a band corresponding to MAP1B is detected. No bands are seen in the liver or non-specific IgG IP sample lanes.

    Techniques Used: Western Blot

    Immunolocalization of MAP1B and Tulp1 in P17 mouse retinas. ( A ) Wt retinal sections stained with MAP1B (red) and Tulp1 (green). ( B ) Tulp1−/− retinal sections stained with MAP1B (red) and Tulp1 (green). Sections were counterstained with DAPI (blue). Scale bar: 50 µm. INL, inner nuclear layer; OPL, outer plexiform layer; ONL, outer nuclear layer; IS, inner segment layer; OS, outer segment layer.
    Figure Legend Snippet: Immunolocalization of MAP1B and Tulp1 in P17 mouse retinas. ( A ) Wt retinal sections stained with MAP1B (red) and Tulp1 (green). ( B ) Tulp1−/− retinal sections stained with MAP1B (red) and Tulp1 (green). Sections were counterstained with DAPI (blue). Scale bar: 50 µm. INL, inner nuclear layer; OPL, outer plexiform layer; ONL, outer nuclear layer; IS, inner segment layer; OS, outer segment layer.

    Techniques Used: Staining



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    IP of retinal lysate. The top panels show Western blot analysis of the <t>MAP1B</t> IP experimental samples probed with Tulp1 antibodies. In the IP product lane, a band corresponding to Tulp1 is detected. A corresponding band is seen in the rat retinal lysate and wt mouse retinal homogenate but not in the tulp1−/− retinal lysate, liver lysate or non-specific IgG IP lanes. The bottom panels show Western blot analysis of the MAP1B IP experimental samples probed with MAP1B antibodies. In the IP product, rat retinal lysate, wt mouse retinal lysate and tulp1−/− retinal lysate lanes, a band corresponding to MAP1B is detected. No bands are seen in the liver or non-specific IgG IP sample lanes.
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    https://www.bioz.com/result/map1b/product/Novus Biologicals
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    IP of retinal lysate. The top panels show Western blot analysis of the <t>MAP1B</t> IP experimental samples probed with Tulp1 antibodies. In the IP product lane, a band corresponding to Tulp1 is detected. A corresponding band is seen in the rat retinal lysate and wt mouse retinal homogenate but not in the tulp1−/− retinal lysate, liver lysate or non-specific IgG IP lanes. The bottom panels show Western blot analysis of the MAP1B IP experimental samples probed with MAP1B antibodies. In the IP product, rat retinal lysate, wt mouse retinal lysate and tulp1−/− retinal lysate lanes, a band corresponding to MAP1B is detected. No bands are seen in the liver or non-specific IgG IP sample lanes.
    Map1b Nb100 68256 Antibody, supplied by Novus Biologicals, 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/result/map1b nb100-68256 antibody/product/Novus Biologicals
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    Image Search Results


    IP of retinal lysate. The top panels show Western blot analysis of the MAP1B IP experimental samples probed with Tulp1 antibodies. In the IP product lane, a band corresponding to Tulp1 is detected. A corresponding band is seen in the rat retinal lysate and wt mouse retinal homogenate but not in the tulp1−/− retinal lysate, liver lysate or non-specific IgG IP lanes. The bottom panels show Western blot analysis of the MAP1B IP experimental samples probed with MAP1B antibodies. In the IP product, rat retinal lysate, wt mouse retinal lysate and tulp1−/− retinal lysate lanes, a band corresponding to MAP1B is detected. No bands are seen in the liver or non-specific IgG IP sample lanes.

    Journal: International Journal of Molecular Sciences

    Article Title: Photoreceptor Compartment-Specific TULP1 Interactomes

    doi: 10.3390/ijms22158066

    Figure Lengend Snippet: IP of retinal lysate. The top panels show Western blot analysis of the MAP1B IP experimental samples probed with Tulp1 antibodies. In the IP product lane, a band corresponding to Tulp1 is detected. A corresponding band is seen in the rat retinal lysate and wt mouse retinal homogenate but not in the tulp1−/− retinal lysate, liver lysate or non-specific IgG IP lanes. The bottom panels show Western blot analysis of the MAP1B IP experimental samples probed with MAP1B antibodies. In the IP product, rat retinal lysate, wt mouse retinal lysate and tulp1−/− retinal lysate lanes, a band corresponding to MAP1B is detected. No bands are seen in the liver or non-specific IgG IP sample lanes.

    Article Snippet: Reciprocal co-IPs were performed on whole rat retina lysate to confirm identified Tulp1-binding partners using the following target antibodies: MAP1B (NB100-68256, Novus Biologicals), Kif3a (EPR5087, Abcam, Cambridge, MA, USA), and Ribeye (612044, BD Transduction, San Francisco, CA, USA).

    Techniques: Western Blot

    Immunolocalization of MAP1B and Tulp1 in P17 mouse retinas. ( A ) Wt retinal sections stained with MAP1B (red) and Tulp1 (green). ( B ) Tulp1−/− retinal sections stained with MAP1B (red) and Tulp1 (green). Sections were counterstained with DAPI (blue). Scale bar: 50 µm. INL, inner nuclear layer; OPL, outer plexiform layer; ONL, outer nuclear layer; IS, inner segment layer; OS, outer segment layer.

    Journal: International Journal of Molecular Sciences

    Article Title: Photoreceptor Compartment-Specific TULP1 Interactomes

    doi: 10.3390/ijms22158066

    Figure Lengend Snippet: Immunolocalization of MAP1B and Tulp1 in P17 mouse retinas. ( A ) Wt retinal sections stained with MAP1B (red) and Tulp1 (green). ( B ) Tulp1−/− retinal sections stained with MAP1B (red) and Tulp1 (green). Sections were counterstained with DAPI (blue). Scale bar: 50 µm. INL, inner nuclear layer; OPL, outer plexiform layer; ONL, outer nuclear layer; IS, inner segment layer; OS, outer segment layer.

    Article Snippet: Reciprocal co-IPs were performed on whole rat retina lysate to confirm identified Tulp1-binding partners using the following target antibodies: MAP1B (NB100-68256, Novus Biologicals), Kif3a (EPR5087, Abcam, Cambridge, MA, USA), and Ribeye (612044, BD Transduction, San Francisco, CA, USA).

    Techniques: Staining