NB100-68256 Search Results


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Novus Biologicals map1b
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 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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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: bioRxiv

Article Title: Photoreceptor Compartment-Specific TULP1 Interactomes

doi: 10.1101/2021.06.07.447411

Figure Lengend Snippet: 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), and Ribeye (612044, BD Transduction).

Techniques: Western Blot

(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: bioRxiv

Article Title: Photoreceptor Compartment-Specific TULP1 Interactomes

doi: 10.1101/2021.06.07.447411

Figure Lengend Snippet: (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), and Ribeye (612044, BD Transduction).

Techniques: Staining