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Myelin Basic Protein (MBP) (68-82), guinea pig

Myelin Basic Protein (MBP) (68-82), guinea pig
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Purity:100%
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Myelin Basic Protein (MBP) (68-82), guinea pig

Catalog No. TP1092Cas No. 98474-59-0
Myelin Basic Protein (MBP) (68-82), guinea pig is a peptide with the sequence Tyr-Gly-Ser-Leu-Pro-Gln-Lys-Ser-Gln-Arg-Ser-Gln-Asp-Glu-Asn.Myelin Basic Protein (MBP) (68-82), guinea pig(MBP (68-82), guinea pig) is a fragment of myelin basic protein (MBP).
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Pack SizePriceAvailabilityQuantity
1 mg$72In Stock
2 mg$97In Stock
5 mg$147In Stock
10 mg$228In Stock
25 mg$389In Stock
50 mg$573In Stock
100 mg$816In Stock
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Product Introduction

Bioactivity
Description
Myelin Basic Protein (MBP) (68-82), guinea pig is a peptide with the sequence Tyr-Gly-Ser-Leu-Pro-Gln-Lys-Ser-Gln-Arg-Ser-Gln-Asp-Glu-Asn.Myelin Basic Protein (MBP) (68-82), guinea pig(MBP (68-82), guinea pig) is a fragment of myelin basic protein (MBP).
In vitro
Multiple sclerosis is the most common autoimmune disorder affecting the central nervous system. The whole blood samples are analyzed for activation capacity and the activatability of CD4+ and CD8+ T-lymphocytes by human total myelin basic protein (MBP), human MBP 104-118 fragment, and guinea pig MBP (68-82) fragment in this study. A significant increase in the number of activated T-lymphocytes was observed in the whole blood. For all three tested MBPs, this increase in activated CD4+ and CD8+ T-lymphocytes is statistically significant (p<0.01). However, this increase in activated T-cells is most prominent following incubation with human total MBP, followed by human 104-118 fragment; the smallest increase is observed following incubation with guinea pig MBP (68-82) fragment (human total MBP>huMBP-104-118>guinea pig MBP (68-82))[1].
In vivo
This study investigates the impact of preemptive bee venom acupuncture (BVA) treatment, starting from the day of myelin basic protein (MBP) (68-82) immunization, on the onset and progression of experimental autoimmune encephalomyelitis (EAE) and associated weight loss. After immunization, rats in the MBP group began showing early signs of EAE, such as partial loss of tail tone, within 5-9 days, progressing to more severe neurological symptoms, including various degrees of limb paralysis, between 10-16 days. In contrast, rats treated with BVA exhibited milder neurological impairments, with a dose-dependent reduction in symptom severity and delayed onset of symptoms (BVA 0.8 mg/kg, 6.4±0.6 days) observed 11-15 days post-immunization. Additionally, the maximum clinical score was significantly lower in the BVA-treated groups (BVA 0.25 mg/kg, 3.7±0.2; BVA 0.8 mg/kg, 2.8±0.3) compared to the untreated MBP group. Moreover, while the MBP group's mean body weight decreased, the MBP + BVA group's mean body weight significantly increased compared to the MBP-only group, highlighting a potential protective effect of BVA against EAE-induced weight loss and symptom severity.
AliasMBP (68-82), guinea pig
Chemical Properties
Molecular Weight1736.79
FormulaC71H113N23O28
Cas No.98474-59-0
Storage & Solubility Information
Storagekeep away from moisture Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Solubility Information
DMSO: 10mM
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM0.5758 mL2.8789 mL5.7577 mL28.7887 mL
5 mM0.1152 mL0.5758 mL1.1515 mL5.7577 mL

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