mouse c peptide elisa kit (ALPCO)
Structured Review
![Plasma from 7-week-old female nonobese diabetes (NOD) and age-, gender, and MHC-matched nonobese diabetes resistant (NOR) mice was evaluated by quantitative immunoblotting for DOC2B protein content. (A) A r epresentative immunoblot is shown from n =10 mice per group. Dashed vertical lines indicate splicing of lanes from within the same gel exposure. Ponceau S served as loading control (37-75 kDa range). (B) Densitometry analysis of the ratio of plasma DOC2B levels (normalized to Ponceau S) in the 7-week-old female NOR versus NOD. (C) Random fasting blood glucose levels were measured in NOR versus NOD mice at 7 weeks of age. (D) Plasma C-peptide levels were assessed using an enzyme-linked immunosorbent assay <t>(ELISA).</t> Data are represented as mean ± SEM; n =10 mice per group; * P <0.05 and n.s.-not significant using one-tailed, unpaired, Student’s t -test for (B), and two-tailed, unpaired, Student’s t -test for [C, D]. (E) DOC2B (magenta), without or with blocking peptide (BP), and insulin (green) immunofluorescence staining; (F) bar graph quantification of DOC2B fluorescence intensity in insulin-positive cells in mouse pancreata, representative of n =4 mice per group. Bar= 10 µm. Merge image contains DOC2B (magenta), insulin (green) and DAPI (blue), nuclear staining. Data represent the mean ± SEM. * P <0.05 by one-tailed, unpaired, Student’s t -test. (G) Quantification of the insulitis scores from hematoxylin-insulin-counterstained pancreatic tissue sections of 7-week-old female NOD and NOR mice, as described in Supplemental Materials and Methods. Data are represented as average mean ± SEM, n =4 mice per group.](https://bio-rxiv-images-cdn.bioz.com/dois_ending_with_10/10__64898_slash_2025__12__28__696610/10__64898_slash_2025__12__28__696610___F3.large.jpg)
Mouse C Peptide Elisa Kit, supplied by ALPCO, used in various techniques. Bioz Stars score: 94/100, based on 140 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/mouse c peptide elisa kit/product/ALPCO
Average 94 stars, based on 140 article reviews
Images
1) Product Images from "Loss of Exocytosis Protein DOC2B is an Early Event in Type 1 Diabetes Development"
Article Title: Loss of Exocytosis Protein DOC2B is an Early Event in Type 1 Diabetes Development
Journal: bioRxiv
doi: 10.64898/2025.12.28.696610
Figure Legend Snippet: Plasma from 7-week-old female nonobese diabetes (NOD) and age-, gender, and MHC-matched nonobese diabetes resistant (NOR) mice was evaluated by quantitative immunoblotting for DOC2B protein content. (A) A r epresentative immunoblot is shown from n =10 mice per group. Dashed vertical lines indicate splicing of lanes from within the same gel exposure. Ponceau S served as loading control (37-75 kDa range). (B) Densitometry analysis of the ratio of plasma DOC2B levels (normalized to Ponceau S) in the 7-week-old female NOR versus NOD. (C) Random fasting blood glucose levels were measured in NOR versus NOD mice at 7 weeks of age. (D) Plasma C-peptide levels were assessed using an enzyme-linked immunosorbent assay (ELISA). Data are represented as mean ± SEM; n =10 mice per group; * P <0.05 and n.s.-not significant using one-tailed, unpaired, Student’s t -test for (B), and two-tailed, unpaired, Student’s t -test for [C, D]. (E) DOC2B (magenta), without or with blocking peptide (BP), and insulin (green) immunofluorescence staining; (F) bar graph quantification of DOC2B fluorescence intensity in insulin-positive cells in mouse pancreata, representative of n =4 mice per group. Bar= 10 µm. Merge image contains DOC2B (magenta), insulin (green) and DAPI (blue), nuclear staining. Data represent the mean ± SEM. * P <0.05 by one-tailed, unpaired, Student’s t -test. (G) Quantification of the insulitis scores from hematoxylin-insulin-counterstained pancreatic tissue sections of 7-week-old female NOD and NOR mice, as described in Supplemental Materials and Methods. Data are represented as average mean ± SEM, n =4 mice per group.
Techniques Used: Clinical Proteomics, Western Blot, Control, Enzyme-linked Immunosorbent Assay, One-tailed Test, Two Tailed Test, Blocking Assay, Immunofluorescence, Staining, Fluorescence
