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This histidine (HIS) tagged human IgG1 F(ab) isotype control is the F(ab) region only and reacts with hen egg lysozyme. It is a recombinant HIS human IgG1 F(ab) produced in CHO cells, designed with low or no specific binding to human samples.
Isotype: Human IgG1, κ
Formulation: PBS, pH 7.0, no stabilizers or preservatives
Endotoxin: ≤0.5 EU/mg
Purity: ≥95% determined by SDS-PAGE
Sterility: 0.2 μm filtration
Molecular Weight: 50 kDa
Storage: Store at 4°C, do not freeze
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More
If you are unable to find the chemical you are looking for, make sure you are logged into your fishersci.com account and click on the following link: eMolecules Building Block Tool
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More
If you are unable to find the chemical you are looking for, make sure you are logged into your fishersci.com account and click on the following link: eMolecules Building Block Tool
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More
A derivative of NNEI in which a fluorine atom has been added to the terminal carbon of the pentyl chain; intended for forensic and research applications
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More
Small and Specialty Supplier Partner Small and/or specialty supplier based on Federal laws and SBA requirements. Learn More
RAS/RAS-RAF-IN-1 is a potent RAS and RAS-RAF inhibitor that exhibits antitumor activity. It demonstrates a KD of 5.0 μM-15 μM for cyclophilin A (CYPA) binding affinity. This compound is intended for research use only.
Potent RAS and RAS-RAF inhibitor
Exhibits antitumor activity
Has a KD of 5.0 μM-15 μM for cyclophilin A (CYPA) binding affinity
Shows EC50 of 0.5 μM-5.0 μM for BRAF-GTP-KRAS-G12C disruption in H358 cells
Demonstrates IC50 of 1.0 μM-10 μM for pERK inhibition in H358 cells
For research use only
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More