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Eglatoprutug Biosimilar – Anti-KIT mAb – Research Grade

Reference:
Size

100ug, 1MG

Isotype

IgG1, kappa

Brand

ProteoGenix

Product type

Primary Antibodies

Clonality

Monoclonal Antibody

Expression system

XtenCHO

Applications

Elisa, WB

Product nameEglatoprutug Biosimilar - Anti-KIT mAb - Research Grade
SpeciesHomo sapiens
Expression systemXtenCHO
Purity>90% by SDS-PAGE.
Buffer0.01M PBS, pH 7.4.
Delivery conditionBlue ice (+4°C)
Delivery Time3-5 days if in stock; 3-5 weeks if production needed
Storage condition4°C for short term; -20°C for long term
BrandProteoGenix
Aliases /Synonymsanti-KIT, Mast/stem cell growth factor receptor Kit, p145 c-kit, Tyrosine-protein kinase Kit, v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog, PBT, Piebald trait protein, Proto-oncogene c-Kit, SCFR, CD117
ReferencePX-TA2061
NoteFor research use only. Not suitable for clinical or therapeutic use.
IsotypeIgG1-kappa
ClonalityMonoclonal Antibody

Description of Eglatoprutug Biosimilar - Anti-KIT mAb - Research Grade

Introduction to Eglatoprutug Biosimilar – Anti-KIT mAb

Eglatoprutug Biosimilar – Anti-KIT mAb is a monoclonal antibody (mAb) that specifically targets the KIT protein. KIT is a receptor tyrosine kinase that plays a crucial role in cell growth, differentiation, and survival. Dysregulation of KIT has been linked to various diseases, including cancer. Eglatoprutug Biosimilar – Anti-KIT mAb is a biosimilar version of the original anti-KIT mAb, designed to have similar structure, activity, and therapeutic applications.

Structure of Eglatoprutug Biosimilar – Anti-KIT mAb

Eglatoprutug Biosimilar – Anti-KIT mAb is a recombinant, fully humanized IgG1 antibody. It is composed of two heavy chains and two light chains, each containing variable and constant regions. The variable regions are responsible for binding to the KIT protein, while the constant regions determine the effector functions of the antibody.

The amino acid sequence of Eglatoprutug Biosimilar – Anti-KIT mAb is highly similar to the original anti-KIT mAb, ensuring its specificity and efficacy. The antibody is produced using mammalian cell culture technology, ensuring high purity and consistency.

Activity of Eglatoprutug Biosimilar – Anti-KIT mAb

Eglatoprutug Biosimilar – Anti-KIT mAb binds to the extracellular domain of the KIT protein with high affinity and specificity. This binding prevents the activation of the KIT receptor, thereby inhibiting downstream signaling pathways involved in cell growth and survival.

In addition to blocking KIT signaling, Eglatoprutug Biosimilar – Anti-KIT mAb also induces antibody-dependent cellular cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC). These effector functions enhance the antibody’s anti-tumor activity by recruiting immune cells to attack KIT-expressing cancer cells.

Application of Eglatoprutug Biosimilar – Anti-KIT mAb

Eglatoprutug Biosimilar – Anti-KIT mAb has shown promising results in preclinical studies and is currently being evaluated in clinical trials for the treatment of KIT-positive cancers. These include gastrointestinal stromal tumors (GISTs), acute myeloid leukemia (AML), and melanoma.

In GISTs, which are the most common KIT-positive cancers, Eglatoprutug Biosimilar – Anti-KIT mAb has demonstrated potent anti-tumor activity, both as a single agent and in combination with other therapies. In AML, the antibody has shown promising results in patients with KIT mutations, who have a poor prognosis and limited treatment options. In melanoma, Eglatoprutug Biosimilar – Anti-KIT mAb has shown potential in combination with other immunotherapies.

Conclusion

Eglatoprutug Biosimilar – Anti-KIT mAb is a biosimilar version of the original anti-KIT mAb, designed to have similar structure, activity, and therapeutic applications. Its highly specific and potent binding to KIT and its effector functions make it a promising therapeutic option for KIT-positive cancers. Clinical trials are ongoing to further evaluate its safety and efficacy, and if successful, Eglatoprutug Biosimilar – Anti-KIT mAb could provide a valuable treatment option for patients with limited options.

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