Tumor Cell Lines

IGR-1

  • For research use only

Cat No.

ABC-TC537S

Product Type

Human Melanoma Cell Lines

Species

Human

Growth Conditions

37 ℃, 5% CO2

Source Organ

Groin Lymph Node

Disease

Melanoma

Product Code

IGR 1; IGR1

IGR-1 human melanoma cells from 42-year-old male show epithelial morphology, BRAF and RAC1 mutations, adherent growth, key for melanoma progression.

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Description

IGR-1 is a human melanoma cell line derived from the inguinal lymph node metastasis of a 42-year-old male patient. The cell line exhibits epithelial-like morphology with adherent growth properties, forming tightly connected monolayers in culture. Genetically, IGR-1 carries oncogenic mutations including BRAF p. Val600Lys and RAC1 p. Pro29Ser, which are key drivers in melanoma pathogenesis and contribute to tumor progression. Cytogenetic analysis confirms the presence of these mutations, reflecting the cell line’s aggressive phenotype. Gene expression profiling indicates dysregulation of signaling pathways downstream of mutated BRAF and RAC1, promoting increased proliferation, migration, and survival. Together, these features make IGR-1 a relevant model for studying melanoma biology and evaluating targeted therapies against BRAF- and RAC1-driven oncogenic signaling.

Product Code

IGR 1; IGR1

Species

Human

Cat.No

ABC-TC537S

Product Category

Tumor Cell Lines

Size/Quantity

1 vial

Growth Mode

Adherent

Shipping Info

Dry Ice

Growth Conditions

37 ℃, 5% CO2

Source Organ

Groin Lymph Node

Disease

Melanoma

Biosafety Level

1

Storage

Liquid Nitrogen

Product Type

Human Melanoma Cell Lines

Application

  • The IGR-1 cell line plays a pivotal role in advancing the understanding of human melanoma biology, particularly in the context of oncogenic signaling, metabolic regulation, and cell proliferation mechanisms. It is widely used to investigate the molecular pathways driven by BRAF and RAC1 mutation, supporting preclinical studies aimed at identifying novel therapeutic targets. Additionally, IGR-1 contributes to crucial insights into melanoma research, researchers could explore drug resistance and evaluate the efficacy of potential therapeutic interventions in melanoma, contributing to the development of more effective treatment strategies.

Citation

When you publish your research, please cite our product as “AcceGen Biotech Cat.# XXX-0000”. In return, we’ll give you a $200 coupon. Simply click here and submit your paper’s PubMed ID (PMID).
Liao Y, Jia X, Ren Y, et al. Suppressive role of microRNA-130b-3p in ferroptosis in melanoma cells correlates with DKK1 inhibition and Nrf2-HO-1 pathway activation. Hum Cell. 2021;34(5):1532-1544. doi:10.1007/s13577-021-00557-5
Gill JG, Leef SN, Ramesh V, et al. A Short Isoform of Spermatogenic Enzyme GAPDHS Functions as a Metabolic Switch and Limits Metastasis in Melanoma. Cancer Res. 2022;82(7):1251-1266. doi:10.1158/0008-5472.CAN-21-2062

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High Viability
To succeed in cell culture
Precision and Reliability
To support a consistent result
Customization Options
Tailed to your research

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