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mouse vasoactive intestinal peptide vip elisa kit  (Cusabio)


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    Structured Review

    Cusabio mouse vasoactive intestinal peptide vip elisa kit
    Hawthorn relieves symptoms of FD in mice. (A1) Body weight,♀; (A2) body weight,♂; (B1) food intake,♀; (B2) food intake,♂; (C1) water consumption,♀; (C2) water consumption,♂; (D) small <t>intestinal</t> propulsion rate; (E) intragastric residual rate; serum NO (F) and GAS (G) levels; <t>VIP</t> (H) , SP (I) , and 5-HT (J) levels in the duodenum. Data are presented as mean ± SD ( n = 10). * p < 0.05, ** p < 0.01.
    Mouse Vasoactive Intestinal Peptide Vip Elisa Kit, supplied by Cusabio, used in various techniques. Bioz Stars score: 92/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mouse+vasoactive+intestinal+peptide+vip+elisa+kit/Mouse+Vasoactive+Intestinal+Peptide%2CVIP+ELISA+Kit/pmc11018912-67-24-32
    Average 92 stars, based on 2 article reviews
    mouse vasoactive intestinal peptide vip elisa kit - by Bioz Stars, 2026-11
    92/100 stars

    Images

    1) Product Images from "Supplementation of Crataegi fructus alleviates functional dyspepsia and restores gut microbiota in mice"

    Article Title: Supplementation of Crataegi fructus alleviates functional dyspepsia and restores gut microbiota in mice

    Journal: Frontiers in Nutrition

    doi: 10.3389/fnut.2024.1385159

    Hawthorn relieves symptoms of FD in mice. (A1) Body weight,♀; (A2) body weight,♂; (B1) food intake,♀; (B2) food intake,♂; (C1) water consumption,♀; (C2) water consumption,♂; (D) small intestinal propulsion rate; (E) intragastric residual rate; serum NO (F) and GAS (G) levels; VIP (H) , SP (I) , and 5-HT (J) levels in the duodenum. Data are presented as mean ± SD ( n = 10). * p < 0.05, ** p < 0.01.
    Figure Legend Snippet: Hawthorn relieves symptoms of FD in mice. (A1) Body weight,♀; (A2) body weight,♂; (B1) food intake,♀; (B2) food intake,♂; (C1) water consumption,♀; (C2) water consumption,♂; (D) small intestinal propulsion rate; (E) intragastric residual rate; serum NO (F) and GAS (G) levels; VIP (H) , SP (I) , and 5-HT (J) levels in the duodenum. Data are presented as mean ± SD ( n = 10). * p < 0.05, ** p < 0.01.

    Techniques Used:

    Related Articles

    Enzyme-linked Immunosorbent Assay:

    Article Title: Supplementation of Crataegi fructus alleviates functional dyspepsia and restores gut microbiota in mice
    Article Snippet: The duodenum of mice was used to prepare tissue homogenate, and 5% of the duodenum homogenate was used to determine the total protein by the BCA method (Nanjing Jiancheng Bioengineering Institute, China, 20210928). .. The 5-hydroxytryptamine (5-HT) ELISA Kit (Wuhan CUSABIO Co., Ltd., L211129838), the Mouse Substance P (SP) ELISA Kit (Wuhan CUSABIO Co., Ltd., L211012768), and the Mouse Vasoactive Intestinal Peptide (VIP) ELISA Kit (Wuhan CUSABIO Co., Ltd., L220113396) were used to determine the 5-HT, SP, and VIP levels in the duodenum. ..

    Article Title: Supplementation of Crataegi fructus alleviates functional dyspepsia and restores gut microbiota in mice.
    Article Snippet: The duodenum of mice was used to prepare tissue homogenate, and 5% of the duodenum homogenate was used to determine the total protein by the BCA method (Nanjing Jiancheng Bioengineering Institute, China, 20210928). .. The 5-hydroxytryptamine (5-HT) ELISA Kit (Wuhan CUSABIO Co., Ltd., L211129838), the Mouse Substance P (SP) ELISA Kit (Wuhan CUSABIO Co., Ltd., L211012768), and the Mouse Vasoactive Intestinal Peptide (VIP) ELISA Kit (Wuhan CUSABIO Co., Ltd., L220113396) were used to determine the 5-HT, SP, and VIP levels in the duodenum. ..



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    Hawthorn relieves symptoms of FD in mice. (A1) Body weight,♀; (A2) body weight,♂; (B1) food intake,♀; (B2) food intake,♂; (C1) water consumption,♀; (C2) water consumption,♂; (D) small <t>intestinal</t> propulsion rate; (E) intragastric residual rate; serum NO (F) and GAS (G) levels; <t>VIP</t> (H) , SP (I) , and 5-HT (J) levels in the duodenum. Data are presented as mean ± SD ( n = 10). * p < 0.05, ** p < 0.01.
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    FIGURE 3 Vasoactive intestinal peptide <t>(VIP)</t> upregulated PTEN, VIP receptor mRNA expression, and Treg‐related cytokines in spleen. Q‐PCR results for VIP mRNA, VIP receptors mRNA expression (A), and PTEN/PI3K/AKT pathway (B) in the spleen. The concentrations of VIP in the serum (C) were measured using <t>ELISA</t> kits (n = 7). The abundance of interleukin (IL)‐10 (D) and IL‐2 (E) in the splenic tissue homogenate supernatant was determined by ELISA as well (n = 7). Unpaired Student t‐test was used in the analysis. *p < 0.05, **p < 0.01, ***p < 0.001.
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    The designed immunization scheme and assay protocol. A total of three oral immunizations were given, and five mice of each group were euthanized for assays <t>of</t> <t>intestinal</t> sIgA and cytokines at weeks 0, 2, 4, 6, 7 and 11 after the first immunization. Serum-specific anti- Trichinella spiralis galectin (Tsgal) antibodies (total IgG, IgG1 and IgG2a) were measured by indirect enzyme-linked immunosorbent assay <t>[ELISA]</t> using recombinant Tsgal (rTsgal) at 2 weeks following each immunization and at weeks 1–5, respectively, following challenge. After being challenged with 300 T. spiralis muscle larvae, 10 mice of each group were sacrificed at weeks 7 and 11 after vaccination (i.e. 7 and 35 days post infection [dpi), and adults worms and muscle larvae were recovered to assess the protective efficacy of recombinant NC8-Tsgal/α-lactose against T. spiralis challenge. Histopathological changes of the intestine and muscles from infected mice were examined at 1 and 5 weeks after challenge (i.e. 7 and 35 dpi). Samples were collected at the time-points indicated in the figure. Ig, Immunoglobulin; IL, interleukin; IFN, interferon; sIgA, secretory (mucosal) IgA
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    Image Search Results


    Differences in gastrointestinal function and fluid metabolism in diarrhea patients with spleen deficiency and dampness. (A) Serum D-xylose levels. (B) Serum gastrin (Gas) levels. (C) Serum vasoactive intestinal peptide (VIP) levels. Statistical significance is indicated as follows: ** p <0.01,*** p <0.001. The experimental groups included ZC (normal group), ZL (standing group), ZLZ (standing combined with lard group), and ZLZS (standing combined with internal and external dampness group).

    Journal: Frontiers in Cellular and Infection Microbiology

    Article Title: External damp environment aggravates diarrhea in spleen deficiency and dampness syndrome in mice: involvement of small intestinal contents microbiota, energy metabolism, gastrointestinal and fluid functions

    doi: 10.3389/fcimb.2024.1495311

    Figure Lengend Snippet: Differences in gastrointestinal function and fluid metabolism in diarrhea patients with spleen deficiency and dampness. (A) Serum D-xylose levels. (B) Serum gastrin (Gas) levels. (C) Serum vasoactive intestinal peptide (VIP) levels. Statistical significance is indicated as follows: ** p <0.01,*** p <0.001. The experimental groups included ZC (normal group), ZL (standing group), ZLZ (standing combined with lard group), and ZLZS (standing combined with internal and external dampness group).

    Article Snippet: The specifications for the ELISA kits used in the analysis are as follows: Mouse Vasoactive Intestinal Peptide (VIP) ELISA Kit (Batch number: JM-02729M2, Jiangsu Jingmei Biotechnology Co., Ltd.), Mouse Gastrin ELISA Kit (Batch number: JM-03140M2, Jiangsu Jingmei Biotechnology Co., Ltd.), Mouse D-xylose ELISA Kit (Batch number: JM-12962M2, Jiangsu Jingmei Biotechnology Co., Ltd.), Mouse Cyclic Guanosine Monophosphate (cGMP) ELISA Kit (Batch number: JM-02304M2, Jiangsu Jingmei Biotechnology Co., Ltd.), and Mouse Cyclic Adenosine Monophosphate (cAMP) ELISA Kit (Batch number: JM-02827M2, Jiangsu Jingmei Biotechnology Co., Ltd.).

    Techniques:

    Hawthorn relieves symptoms of FD in mice. (A1) Body weight,♀; (A2) body weight,♂; (B1) food intake,♀; (B2) food intake,♂; (C1) water consumption,♀; (C2) water consumption,♂; (D) small intestinal propulsion rate; (E) intragastric residual rate; serum NO (F) and GAS (G) levels; VIP (H) , SP (I) , and 5-HT (J) levels in the duodenum. Data are presented as mean ± SD ( n = 10). * p < 0.05, ** p < 0.01.

    Journal: Frontiers in Nutrition

    Article Title: Supplementation of Crataegi fructus alleviates functional dyspepsia and restores gut microbiota in mice

    doi: 10.3389/fnut.2024.1385159

    Figure Lengend Snippet: Hawthorn relieves symptoms of FD in mice. (A1) Body weight,♀; (A2) body weight,♂; (B1) food intake,♀; (B2) food intake,♂; (C1) water consumption,♀; (C2) water consumption,♂; (D) small intestinal propulsion rate; (E) intragastric residual rate; serum NO (F) and GAS (G) levels; VIP (H) , SP (I) , and 5-HT (J) levels in the duodenum. Data are presented as mean ± SD ( n = 10). * p < 0.05, ** p < 0.01.

    Article Snippet: The 5-hydroxytryptamine (5-HT) ELISA Kit (Wuhan CUSABIO Co., Ltd., L211129838), the Mouse Substance P (SP) ELISA Kit (Wuhan CUSABIO Co., Ltd., L211012768), and the Mouse Vasoactive Intestinal Peptide (VIP) ELISA Kit (Wuhan CUSABIO Co., Ltd., L220113396) were used to determine the 5-HT, SP, and VIP levels in the duodenum.

    Techniques:

    FIGURE 3 Vasoactive intestinal peptide (VIP) upregulated PTEN, VIP receptor mRNA expression, and Treg‐related cytokines in spleen. Q‐PCR results for VIP mRNA, VIP receptors mRNA expression (A), and PTEN/PI3K/AKT pathway (B) in the spleen. The concentrations of VIP in the serum (C) were measured using ELISA kits (n = 7). The abundance of interleukin (IL)‐10 (D) and IL‐2 (E) in the splenic tissue homogenate supernatant was determined by ELISA as well (n = 7). Unpaired Student t‐test was used in the analysis. *p < 0.05, **p < 0.01, ***p < 0.001.

    Journal: Immunity, inflammation and disease

    Article Title: Vasoactive intestinal peptide exerts therapeutic action by regulating PTEN in a model of Sjögren's disease.

    doi: 10.1002/iid3.936

    Figure Lengend Snippet: FIGURE 3 Vasoactive intestinal peptide (VIP) upregulated PTEN, VIP receptor mRNA expression, and Treg‐related cytokines in spleen. Q‐PCR results for VIP mRNA, VIP receptors mRNA expression (A), and PTEN/PI3K/AKT pathway (B) in the spleen. The concentrations of VIP in the serum (C) were measured using ELISA kits (n = 7). The abundance of interleukin (IL)‐10 (D) and IL‐2 (E) in the splenic tissue homogenate supernatant was determined by ELISA as well (n = 7). Unpaired Student t‐test was used in the analysis. *p < 0.05, **p < 0.01, ***p < 0.001.

    Article Snippet: Serum extraction method as published,20 VIP levels in serum were measured using the mouse VIP ELISA kit (Elabscience).

    Techniques: Expressing, Enzyme-linked Immunosorbent Assay

    The designed immunization scheme and assay protocol. A total of three oral immunizations were given, and five mice of each group were euthanized for assays of intestinal sIgA and cytokines at weeks 0, 2, 4, 6, 7 and 11 after the first immunization. Serum-specific anti- Trichinella spiralis galectin (Tsgal) antibodies (total IgG, IgG1 and IgG2a) were measured by indirect enzyme-linked immunosorbent assay [ELISA] using recombinant Tsgal (rTsgal) at 2 weeks following each immunization and at weeks 1–5, respectively, following challenge. After being challenged with 300 T. spiralis muscle larvae, 10 mice of each group were sacrificed at weeks 7 and 11 after vaccination (i.e. 7 and 35 days post infection [dpi), and adults worms and muscle larvae were recovered to assess the protective efficacy of recombinant NC8-Tsgal/α-lactose against T. spiralis challenge. Histopathological changes of the intestine and muscles from infected mice were examined at 1 and 5 weeks after challenge (i.e. 7 and 35 dpi). Samples were collected at the time-points indicated in the figure. Ig, Immunoglobulin; IL, interleukin; IFN, interferon; sIgA, secretory (mucosal) IgA

    Journal: Parasites & Vectors

    Article Title: Oral immunization of mice with recombinant Lactobacillus plantarum expressing a Trichinella spiralis galectin induces an immune protection against larval challenge

    doi: 10.1186/s13071-022-05597-w

    Figure Lengend Snippet: The designed immunization scheme and assay protocol. A total of three oral immunizations were given, and five mice of each group were euthanized for assays of intestinal sIgA and cytokines at weeks 0, 2, 4, 6, 7 and 11 after the first immunization. Serum-specific anti- Trichinella spiralis galectin (Tsgal) antibodies (total IgG, IgG1 and IgG2a) were measured by indirect enzyme-linked immunosorbent assay [ELISA] using recombinant Tsgal (rTsgal) at 2 weeks following each immunization and at weeks 1–5, respectively, following challenge. After being challenged with 300 T. spiralis muscle larvae, 10 mice of each group were sacrificed at weeks 7 and 11 after vaccination (i.e. 7 and 35 days post infection [dpi), and adults worms and muscle larvae were recovered to assess the protective efficacy of recombinant NC8-Tsgal/α-lactose against T. spiralis challenge. Histopathological changes of the intestine and muscles from infected mice were examined at 1 and 5 weeks after challenge (i.e. 7 and 35 dpi). Samples were collected at the time-points indicated in the figure. Ig, Immunoglobulin; IL, interleukin; IFN, interferon; sIgA, secretory (mucosal) IgA

    Article Snippet: The levels of intestinal histamine concentrations were measured using a mouse ELISA kit according to the manufacturer's instructions (Elabscience Biotechnol, Wuhan, China).

    Techniques: Indirect ELISA, Enzyme-linked Immunosorbent Assay, Recombinant, Infection, Muscles