d ap5 (Hello Bio Inc)
Structured Review

D Ap5, supplied by Hello Bio Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/d ap5/product/Hello Bio Inc
Average 86 stars, based on 1 article reviews
Images
1) Product Images from "Protocol for whole-cell patch-clamp recording and post hoc identification of hippocampal CA2 pyramidal neurons in adult mouse brain slices"
Article Title: Protocol for whole-cell patch-clamp recording and post hoc identification of hippocampal CA2 pyramidal neurons in adult mouse brain slices
Journal: STAR Protocols
doi: 10.1016/j.xpro.2026.104470
Figure Legend Snippet: Passive properties of CA2 pyramidal neurons and miniature IPSCs (A) Capacitive and leakage currents in a CA2 pyramidal neuron in response to a 5 mV voltage step recorded at a holding potential of Vh=−70 mV before the current trace in A. The series resistance Rs is 8.1 MΩ. Capacitive transients are fitted with the sum of two exponentials giving time constants of 30 and 355 pF. Read out value from clampEx was Cm=210 pF. Current trace is an average of 9 raw traces. (B) Capacitive and leakage currents acquired after the current trace in C to show the absence of gross change in the passive properties of the cell and recording conditions. Rs is 8.8 MΩ (less than 9% change in comparison to condition in A). Average current trace from 11 raw traces. Current traces in A and B are recorded in the presence of 20 μM D-AP5, 10 μM CNQX, and 1 μM TTX.
Techniques Used: Comparison
Figure Legend Snippet: Excitatory and inhibitory spontaneous synaptic currents in CA2 pyramidal neurons (A) Representative recording of mIPSCs at a holding potential of Vh=−70 mV. 20 μM D-AP5, 10 μM CNQX, and 1 μM TTX are added to external solution to block excitatory synaptic activity and spontaneous AP firing. Green dashed vertical lines indicate the sections of current selected for expanded time view in B. Current trace sections are labeled #1 to #5. (B) Selection of five current trace sections extracted from current trace in (C). (C) Miniature currents selected using Clampfit with template matching selection method. Superimposition of 23 individual current traces in black with one in red. (D) Current traces from (C) at expanded time scale. (E) Original trace of sEPSCs recorded at a holding potential of Vh=−70 mV. 50 μM picrotoxin was added to external solution to block inhibitory synaptic activity. Blue dashed vertical lines indicate the sections of current selected for expanded time view in F. (F) Five current trace segments (blue label #1 to #5) extracted from the whole current trace in (E) at expanded time scale. (G) Spontaneous excitatory postsynaptic currents selected using Clampfit with template matching selection method. Superimposition of 12 individual current traces in black with one in red. (H) Current traces from (G) at expanded time scale.
Techniques Used: Blocking Assay, Activity Assay, Labeling, Selection
