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horizontal dmz universal puller  (Carl Zeiss)


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    Structured Review

    Carl Zeiss horizontal dmz universal puller
    Horizontal Dmz Universal Puller, supplied by Carl Zeiss, 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/product/horizontal+dmz+universal+puller/440+electron+leo+microscope+scanning/pmc08634576-94-5-9
    Average 90 stars, based on 1 article reviews
    horizontal dmz universal puller - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    other:

    Article Title: Electrophysiological and Molecular Characterization of the Parasubiculum
    Article Snippet: 220 Pipettes were pulled using a horizontal DMZ Universal Puller (Zeiss, Germany).

    Article Title: Electrophysiological and Molecular Characterization of the Parasubiculum
    Article Snippet: Somatic whole-cell recordings were performed using glass pipettes pulled from borosilicate glass capillaries with a tip resistance of 3–6 m Ω. Pipettes were pulled using a horizontal DMZ Universal Puller (Carl Zeiss).



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    (A) Structural model of the CNBD of HCN channels. The 2 key residues R591 (yellow) and T592 (pink) that are crucial for binding of cAMP are highlighted. (B) <t>Horizontal</t> brain slices of WT and HCN2EA mice. The position of the dLGN (red) and the VB (blue) is indicated. (C) Detection of HCN2 and HCN4 in Western blot analysis of punched dLGN and VB regions. Images are representatives of n = 3/group. (D) Western blot analysis of membrane preparations of HCN2EA and WT mice probed for HCN2 and a loading control (Na+/K+-ATPase). Images are representatives of n = 3/group. (E) Quantification of HCN2 expression level in relation to the Na+/K+-ATPase (n = 3).
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    Image Search Results


    (A) Structural model of the CNBD of HCN channels. The 2 key residues R591 (yellow) and T592 (pink) that are crucial for binding of cAMP are highlighted. (B) Horizontal brain slices of WT and HCN2EA mice. The position of the dLGN (red) and the VB (blue) is indicated. (C) Detection of HCN2 and HCN4 in Western blot analysis of punched dLGN and VB regions. Images are representatives of n = 3/group. (D) Western blot analysis of membrane preparations of HCN2EA and WT mice probed for HCN2 and a loading control (Na+/K+-ATPase). Images are representatives of n = 3/group. (E) Quantification of HCN2 expression level in relation to the Na+/K+-ATPase (n = 3).

    Journal: JCI Insight

    Article Title: Abolishing cAMP sensitivity in HCN2 pacemaker channels induces generalized seizures

    doi: 10.1172/jci.insight.126418

    Figure Lengend Snippet: (A) Structural model of the CNBD of HCN channels. The 2 key residues R591 (yellow) and T592 (pink) that are crucial for binding of cAMP are highlighted. (B) Horizontal brain slices of WT and HCN2EA mice. The position of the dLGN (red) and the VB (blue) is indicated. (C) Detection of HCN2 and HCN4 in Western blot analysis of punched dLGN and VB regions. Images are representatives of n = 3/group. (D) Western blot analysis of membrane preparations of HCN2EA and WT mice probed for HCN2 and a loading control (Na+/K+-ATPase). Images are representatives of n = 3/group. (E) Quantification of HCN2 expression level in relation to the Na+/K+-ATPase (n = 3).

    Article Snippet: A horizontal puller (DMZ Universal Electrode Puller, Zeitz-Instruments) was used to pull patch pipettes from borosilicate glass tubing (GC150TF-10, Harvard Apparatus).

    Techniques: Binding Assay, Western Blot, Membrane, Control, Expressing