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G6PI 325-339 (human) hydrochloride is an effective inducer of arthritis in B10.Q mice. It triggers cross-reactivity of Th1 and Th17 cells with mouse G6PI protein. This compound induces an arthritis model through T and B cell-dependent pathways, without involving any antibody effector mechanisms.
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| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | G6PI 325-339 (human) hydrochloride is an effective inducer of arthritis in B10.Q mice. It triggers cross-reactivity of Th1 and Th17 cells with mouse G6PI protein. This compound induces an arthritis model through T and B cell-dependent pathways, without involving any antibody effector mechanisms. |
| In vivo | The compound G6PI is involved in the induction of an arthritis model. G6PI can generate antibodies in vivo, triggering immune cells to produce cytokines (such as TNF-α and IL-1β), which can lead to arthritis. Model induction in mice involves using 50 μg of complete Freund's adjuvant administered as a single subcutaneous injection at the base of the tail in 6-10 week-old DBA/1 mice. Note: (1) DBA/1 mice are raised in our facility under specific pathogen-free conditions. (2) Mice are euthanized on day 12 post-immunization to prepare draining lymph node single-cell suspensions. Successful modeling indicators include morphological signs such as pronounced synovitis and adjacent skeletal muscle inflammation predominated by neutrophils, a hallmark of acute inflammation, with mild activation of synovial fibroblasts. The synovial tissue swells due to inflammatory infiltration; however, bone damage is only locally visible. On a molecular level, there are increased levels of IL-17, TNFα, RANKL, and IFNγ. |
| Synonyms | hG6PI (325-339) hydrochloride |
| Formula | C82H118ClN19O21S3.xHCl |
| Sequence | Ile-Trp-Tyr-Ile-Asn-Cys-Phe-Gly-Cys-Glu-Thr-His-Ala-Met-Leu |
| Sequence Short | IWYINCFGCETHAML |
| Storage | keep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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