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Creative Biolabs

NeuroMab™ Anti-IL-6 Antibody(NRP-0422-P1510)

[CAT#: NRP-0422-P1510]

Functional antibody against Human IL-6

Host Species:
Humanized
Species Reactivity:
Human
Applications:
In Vitro; In Vivo; Antagonist

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Product Overview

Description

NRP-0422-P1510 is a humanized anti-interleukin-6 (anti-IL-6) monoclonal immunoglobulin 1 (IgG1) antibody, and can be administered as a non-erythropoietic stimulating agent for treating cancer-related anemia.

Species Reactivity

Human

Clonality

Monoclonal

Host Species

Humanized

Applications

In Vitro; In Vivo; Antagonist

Relevant Diseases

Neuroinflammation
Product Properties

Formulation

PBS only

Preservatives

BSA Free

Concentration

1mg/mL

Purification

Purified recombinant IgG prepared by affinity chromatography on Protein A from a mammalian cell line

Purity

> 95% (SDS-PAGE)

Endotoxin Level

Regular Endotoxin < 5 EU/mg
Low Endotoxin < 1 EU/mg

Shipping

Gel Packs

Storage

Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.

Research Use Only

For research use only
Target

Target

IL-6

Official Name

IL6

Full Name

Interleukin 6 (IL-6)

Alternative Names

IL6; BSF2; HGF; HSF; IFNB2; IL-6; BSF-2; CDF; IFN-beta-2; interleukin 6

Gene ID

3569(Human)

Uniprot ID

P05231(Human)
Product Pictures
FuncS

Figure 1 depicts mean plasma CRP concentrations following a single intravenous injection in patients with advanced cancer. Ab1 (ALD518) was infused at 80, 160 or 320 mg (n=8).

FuncS

Figure 2 depicts mean serum CRP levels in rheumatoid arthritis patients with an inadequate response to methotrexate following administration of 80, 160, or 320 mg of Ab1(ALD518).

FuncS

Figure 3 shows that Ab1 increased mean hemoglobin concentration (g/dL) by 80, 160 and 320 mg after 12 weeks of administration in NSCLC patients compared to placebo.

FuncS

Figure 4 depicts Ab1 increasing mean albumin concentrations at 80, 160 and 320 mg in NSCLC patients.

FuncS

Figure 5 graphically illustrates the mean change in SF-36 composite score at week 12 in a phase II clinical trial of ALD518 administered to patients with active RA.

FuncS

Figure 6 depicts the relationship between WHO oral mucositis grade and cumulative IMRT (Gy): Three patients received ALD518 160 mg intravenously at weeks 0 and 4.

Publications

Publications (0)

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