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中文名称:小鼠颗粒酶B(Gzms-B)酶联免疫试剂盒
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货号:CSB-E08720m
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规格:96T/48T
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价格:¥3800/¥2500
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其他:
产品详情
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产品描述:
This Mouse GZMB ELISA Kit was designed for the quantitative measurement of Mouse GZMB protein in serum, plasma, tissue homogenates. It is a Sandwich ELISA kit, its detection range is 12.5 pg/mL-800 pg/mL and the sensitivity is 3.12 pg/mL.
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别名:Gzmb ELISA kit; Ctla-1 ELISA kit; Ctla1Granzyme B(G,H ELISA kit; EC 3.4.21.79 ELISA kit; CTLA-1 ELISA kit; Cytotoxic cell protease 1 ELISA kit; CCP1 ELISA kit; Fragmentin-2 ELISA kit
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缩写:
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Uniprot No.:
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种属:Mus musculus (Mouse)
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样本类型:serum, plasma, tissue homogenates
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检测范围:12.5 pg/mL-800 pg/mL
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灵敏度:3.12 pg/mL
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反应时间:1-5h
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样本体积:50-100ul
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检测波长:450 nm
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研究领域:Cell Biology
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测定原理:quantitative
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测定方法:Sandwich
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精密度:
Intra-assay Precision (Precision within an assay): CV%<8% Three samples of known concentration were tested twenty times on one plate to assess. Inter-assay Precision (Precision between assays): CV%<10% Three samples of known concentration were tested in twenty assays to assess. -
线性度:
To assess the linearity of the assay, samples were spiked with high concentrations of mouse Gzms-B in various matrices and diluted with the Sample Diluent to produce samples with values within the dynamic range of the assay. Sample Serum(n=4) 1:1 Average % 102 Range % 95-106 1:2 Average % 86 Range % 82-92 1:4 Average % 94 Range % 89-98 1:8 Average % 95 Range % 89-99 -
回收率:
The recovery of mouse Gzms-B spiked to levels throughout the range of the assay in various matrices was evaluated. Samples were diluted prior to assay as directed in the Sample Preparation section. Sample Type Average % Recovery Range Serum (n=5) 103 96-107 EDTA plasma (n=4) 93 88-97 -
标准曲线:
These standard curves are provided for demonstration only. A standard curve should be generated for each set of samples assayed. pg/ml OD1 OD2 Average Corrected 800 2.076 2.143 2.110 1.985 400 1.723 1.812 1.768 1.643 200 1.262 1.292 1.277 1.152 100 0.783 0.796 0.790 0.665 50 0.402 0.415 0.409 0.284 25 0.276 0.280 0.278 0.153 12.5 0.191 0.195 0.193 0.068 0 0.124 0.126 0.125 -
数据处理:
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货期:3-5 working days
引用文献
- Icaritin-curcumol activates CD8+ T cells through regulation of gut microbiota and the DNMT1/IGFBP2 axis to suppress the development of prostate cancer W Xu,Journal of experimental & clinical cancer research,2024
- Synergistic Antineoplastic and Immunomodulatory Effects of Hesperidin in Ehrlich Ascites Carcinoma Tumor Model Treated with Cisplatin HM Abd El Latif,/,2024
- Astragaloside IV-PESV Repressed T Cell Immunosuppression by Inhibiting PD-L1 Expression in Prostate Cancer through STAT3 Pathway X You,Journal of Food Biochemistry,2023
- Immunization with the amino-terminus region of dense granule protein 6 (GRA6) of Toxoplasma gondii activates CD8+ cytotoxic T cells capable of removing tissue cysts of the parasite through antigen presentation by human HLA-A2.1 R Mani,Microbes and infection,2023
- Immunomodulatory, apoptotic and anti-proliferative potentials of sildenafil in Ehrlich ascites carcinoma murine model: In vivo and in silico insights DS Morsi,International immunopharmacology,2023
- In vitro effect of 4-pentylphenol and 3-methyl-4-nitrophenol on murine splenic lymphocyte populations and cytokine/granzyme production. Yang L.et al,J Immunotoxicol.,2016
- Walnut Polyphenol Extract Attenuates Immunotoxicity Induced by 4-Pentylphenol and 3-methyl-4-nitrophenol in Murine Splenic Lymphocyte Yang L.et al,Nutrients.,2016
- Alpha-fetoprotein Epitope Peptide Promoted the Proliferation of Primary Hepatocellular Carcinoma Cells H Lin. et al,/,2015
相关产品
靶点详情
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功能:Abundant protease in the cytosolic granules of cytotoxic T-cells and NK-cells which activates caspase-independent pyroptosis when delivered into the target cell through the immunological synapse. It cleaves after Asp. Once delivered into the target cell, acts by catalyzing cleavage of gasdermin-E (GSDME), releasing the pore-forming moiety of GSDME, thereby triggering pyroptosis and target cell death. Seems to be linked to an activation cascade of caspases (aspartate-specific cysteine proteases) responsible for apoptosis execution. Cleaves caspase-3, -7, -9 and 10 to give rise to active enzymes mediating apoptosis.
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基因功能参考文献:
- Tcf1 binding reduced the activity of a Gzmb-associated regulatory element, and this accounted for the reduced Gzmb expression in Tcf1-expressing NK cells. PMID: 28723565
- Differential proteomics were used to identify granzyme B substrates in three unrelated bacteria: Escherichia coli, Listeria monocytogenes, and Mycobacteria tuberculosis. Granzyme B cleaves a highly conserved set of proteins in all three bacteria, which function in vital biosynthetic and metabolic pathways that are critical for bacterial survival under diverse environmental conditions. PMID: 29107333
- Released granzyme B induces DNA fragmentation in intraepithelial lymphocytes independently of Perforin PMID: 25750028
- serglycin plays a critical role in the maturation of dense-core cytotoxic granules in cytotoxic lymphocytes and the trafficking and storage of perforin and granzyme B, whereas granzyme A is unaffected PMID: 26756195
- these results suggest a perforin-independent, extracellular role for GzmB in the pathogenesis of cardiac fibrosis PMID: 26610869
- data indicate an involvement of granzyme B in the neuroinflammation mediated by Eomes(+) CD4(+) T cells. PMID: 26436530
- Data suggest that targeting granzyme B (GzmB) in selected T cell subsets may provide a strategy to control graft-versus-host disease (GVHD). PMID: 26392464
- We conclude that GzmbCre can be used under some conditions to investigate gene function in mature and activated natural killer cells. PMID: 25923440
- These findings indicate a significant role for GzmB in extracellular matrix degradation that may have implications in many age-related chronic inflammatory diseases. PMID: 25495009
- Different natural variants of granzyme B have a profound impact on the immune response to a common and authentic viral pathogen. PMID: 25502180
- Visualization of granzyme B-expressing CD8 T cells during primary and secondary immune responses to Listeria monocytogenes. PMID: 25367158
- expedites cytotoxic T-lymphocyte diapedesis via basement membrane remodeling PMID: 25526309
- CD4(+) natural killer cells potently promote atherosclerosis by granzyme B (and perforin)-dependent apoptosis. PMID: 25398236
- Granzyme B has a role in atherosclerotic plaque development. PMID: 24205352
- Data indicate that vascular permeability is reduced in Granzyme B (GZMB)-KO mice after delayed-type hypersensitivity -induced inflammation. PMID: 24791744
- GzmB is a negative regulator of hematopoietic stem cell function that is induced by stress and chemotherapy in both HSCs and their niches. PMID: 24752302
- studies established a pivotal role for NK-cell NKG2D and granzyme B in the pathogenesis of house dust mite-allergic lung disease, and identified novel therapeutic targets for the prevention and treatment of asthma. PMID: 24290277
- The apoptotic cell-in-cell death occurred only in internalized immune killer cells expressing granzyme B PMID: 24113190
- Granzyme B deficiency exacerbates lung inflammation in mice after acute lung injury. PMID: 23642129
- Genetic deletion of granzyme B does not confer resistance to the development of spontaneous diabetes in non-obese diabetic mice. PMID: 23663075
- in the Period 1 gene (Per1(-/-) mice), involved in the negative limb of the molecular clock, display significantly altered rhythms of cytokine (eg, interferon-gamma) and cytolytic factors (eg, perforin and granzyme B) in splenic natural killer (NK) cells. PMID: 23402528
- granzyme B is dispensable for beta cell destruction in type 1 diabetes, but is required for efficient early activation of cytotxic T lymphocytes. PMID: 22792290
- GzmB-mediated, activation-induced cell death in wild-type T8 cells was responsible for their reduced graft-vs-tumor activity. GzmB(-/-) T8 cells had enhanced expansion, skewed toward an effector/memory phenotype, & made more IFN-gamma & Fas ligand. PMID: 23264653
- expression by regulatory t-cells controls lung inflammation during acute viral infection PMID: 22236998
- There is a role for Granzyme B in age-related skin thinning and frailty. PMID: 21316440
- Data suggest that an interdependent relationship between parasite burden and CD8(+) T cells dictates the onset of perforin/GzmB-mediated ECM. PMID: 21525386
- During lymphocytic choriomeningitis virus infection, despite persistent similarities in chromatin of CD8-positive memory cells, continuous transcription does not occur at the granzyme B locus. PMID: 21278341
- GzmA/B deficiency in filarial infection is associated with a defense-promoting Th2 cytokine and antibody shift, enhanced early inflammatory gene expression, and a trend of reduced alternatively activated macrophage induction. PMID: 21248253
- The herpes simplex virus type 1 LAT protects neuron cells from granzyme B-induced apoptosis and CD8 T-cell killing. PMID: 21177822
- miR-223 specifically targets the 3' untranslated region of murine GzmB in vitro, indicating that this miRNA may contribute to control of GzmB translation in resting NK cells. PMID: 20935160
- Data show that increased activation-induced apoptosis resulted in impaired survival and a decreased clonal burst size of Spi6 KO iNKT cells, which could be corrected by GrB deficiency. PMID: 20543105
- Surprisingly, adoptive transfer of granzyme B-deficient T(reg) cells prevented GVHD lethality, suppressed serum cytokine production in vivo, and prevented target organ damage. PMID: 19965675
- Pathogenetically relevant immune reactions in proteolipid protein-overexpressing mice are TCR-dependent and mediated by the classical components of CD8+ T-cell cytotoxicity, perforin, and Gzmb. PMID: 20042681
- gzmB has a role in caspase-dependent inhibition of mousepox replication PMID: 19838298
- In all tumor models examined thus far, granzyme B is not necessary for tumor rejection mediated by the perforin pathway in vivo. PMID: 12847210
- Granzyme-mediated cytotoxicity does not involve the mannose 6-phosphate receptors on target cells PMID: 14985351
- Granzyme-B is one of the key mechanisms through which CD4+CD25+ regulatory T cells induce cell contact-mediated suppression. PMID: 15699103
- polymorphonuclear leukocytes from mice and humans lack the 3 cytotoxic effector molecules, granzyme A, granzyme B, and perforin, generally associated with natural killer and cytotoxic T lymphocytes PMID: 15998831
- suppression of natural killer cell activity induced by whole body hyperthermia could be mediated through the perforin/granzyme pathway PMID: 16236268
- In this study, we discuss our recent findings on granzyme B-induced cell death and discuss the potential relevance of this pathway to CL-induced death of viral-infected and transformed cells. PMID: 16405654
- absence of either perforin or granzyme B resulted in cell survival in alloreactive CTL-induced pancreatic beta cells PMID: 16436955
- GrB plays a critical role in the T cell receptor-induced cell death of Th2 cells PMID: 16901729
- Hop may be cleaved by GzmB as an "innocent bystander" during the induction of apoptosis, but it may also act to facilitate apoptosis in concert with other GzmB substrates PMID: 17005566
- Granzyme B expression is augmented in activated T cells from Bcl6-/- knockout mice. PMID: 17125145
- Varies considerably more in wild populations (2-18 amino acid differences) than between common laboratory strains (12 of 13 were identical). PMID: 17661907
- This is the first report of a major distal regulatory element in the control of granzyme B transcription. PMID: 18222115
- For the first time, in vivo data implicate granzyme B expression by regulatory T (Treg) lymphocytes in sustaining long-lived graft survival. PMID: 18802078
- In vitro protease substrate profiling of the apoptotic serine protease granzyme B was performed resulting in the delineation of more than 800 cleavage sites in 322 human and 282 mouse substrates PMID: 18836177
- granzyme C is activated with persistent antigenic stimulation, providing nonredundant backup protection for the host when granzyme B fails. PMID: 19414782
- for high levels of transcription to occur a distinct set of histone modifications needs to be established in addition to histone loss at the proximal promoter of gzmB PMID: 19915065
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亚细胞定位:Secreted. Cytolytic granule.
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蛋白家族:Peptidase S1 family, Granzyme subfamily
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数据库链接:
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