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biotin conjugated pha e  (Vector Laboratories)


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    Vector Laboratories biotin conjugated pha e
    Biotin Conjugated Pha E, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 93/100, based on 72 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/biotin+conjugated+pha+e/pm40400458-217-17-22?v=Vector+Laboratories
    Average 93 stars, based on 72 article reviews
    biotin conjugated pha e - by Bioz Stars, 2026-07
    93/100 stars

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    A lectin blot of whole cell lysates from NB cells with (NB_1), and without Mgat2 (NB_1(- Mgat2 )), and also, the NB_1(- Mgat2) cell line transiently transfected with Mgat2 to create the rescued cell line, called NB_1(-/+ Mgat2 ) (A) . Proteins separated on membranes were probed with <t>Phaseolus</t> <t>vulgaris</t> Erthroagglutinin <t>(E-PHA)</t> or Phaseolus vulgaris Leucoagglutinin (L-PHA). Coomassie blue stained SDS gels reflect similar amounts of protein per lane. Lines adjacent to blot and gel indicate molecular weight standards in kDa: 250, 150, 100, 75, 50, and 37 from top to bottom. Western blot of total membranes from NB_1, NB_1(- Mgat2 ), and NB_1(-/+ Mgat2 ) cell lines transfected with glycosylated (WT) and unglycosylated (DM) Kv3.1b (B) . (+) indicates the cell line examined. Black and gray arrows represent complex and hybrid types of N-glycans, respectively, attached to Kv3.1b. The gray dotted line indicates oligomannose type glycans attached to Kv3.1b, and the black line denotes unglycosylated Kv3.1b. Molecular weight markers adjacent to the membranes are in kDa.
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    A lectin blot of whole cell lysates from NB cells with (NB_1), and without Mgat2 (NB_1(- Mgat2 )), and also, the NB_1(- Mgat2) cell line transiently transfected with Mgat2 to create the rescued cell line, called NB_1(-/+ Mgat2 ) (A) . Proteins separated on membranes were probed with Phaseolus vulgaris Erthroagglutinin (E-PHA) or Phaseolus vulgaris Leucoagglutinin (L-PHA). Coomassie blue stained SDS gels reflect similar amounts of protein per lane. Lines adjacent to blot and gel indicate molecular weight standards in kDa: 250, 150, 100, 75, 50, and 37 from top to bottom. Western blot of total membranes from NB_1, NB_1(- Mgat2 ), and NB_1(-/+ Mgat2 ) cell lines transfected with glycosylated (WT) and unglycosylated (DM) Kv3.1b (B) . (+) indicates the cell line examined. Black and gray arrows represent complex and hybrid types of N-glycans, respectively, attached to Kv3.1b. The gray dotted line indicates oligomannose type glycans attached to Kv3.1b, and the black line denotes unglycosylated Kv3.1b. Molecular weight markers adjacent to the membranes are in kDa.

    Journal: PLoS ONE

    Article Title: Lack of complex type N-glycans lessens aberrant neuronal properties

    doi: 10.1371/journal.pone.0199202

    Figure Lengend Snippet: A lectin blot of whole cell lysates from NB cells with (NB_1), and without Mgat2 (NB_1(- Mgat2 )), and also, the NB_1(- Mgat2) cell line transiently transfected with Mgat2 to create the rescued cell line, called NB_1(-/+ Mgat2 ) (A) . Proteins separated on membranes were probed with Phaseolus vulgaris Erthroagglutinin (E-PHA) or Phaseolus vulgaris Leucoagglutinin (L-PHA). Coomassie blue stained SDS gels reflect similar amounts of protein per lane. Lines adjacent to blot and gel indicate molecular weight standards in kDa: 250, 150, 100, 75, 50, and 37 from top to bottom. Western blot of total membranes from NB_1, NB_1(- Mgat2 ), and NB_1(-/+ Mgat2 ) cell lines transfected with glycosylated (WT) and unglycosylated (DM) Kv3.1b (B) . (+) indicates the cell line examined. Black and gray arrows represent complex and hybrid types of N-glycans, respectively, attached to Kv3.1b. The gray dotted line indicates oligomannose type glycans attached to Kv3.1b, and the black line denotes unglycosylated Kv3.1b. Molecular weight markers adjacent to the membranes are in kDa.

    Article Snippet: Biotin-conjugated Phaseolus vulgaris Erythoagglutinin (E-PHA) or Phaseolus vulgaris Leucoagglutinin (L-PHA) (Vector Laboratories, CA, USA) was employed to probe membranes containing separated glycosylated proteins.

    Techniques: Transfection, Staining, Molecular Weight, Western Blot