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Key Features

Anti-Mouse PD-1 (CD279) [RMP1-14] In Vivo Antibody - Ultra Low Endotoxin (IVMB0038)

SKU IVMB0038
Antibody Type Functional-Grade In Vivo Antibody
Applications In Vivo
Disease Area Cancer Immunotherapy
Disease Area Autoimmune Diseases
Clone RMP1-14
Protein PD-1
Isotype Rat IgG2a kappa
Reactivity Mouse
Synonyms Programmed Death-1
Synonyms CD279
Synonyms PD 1
Research Area Immune Checkpoint & Cancer Biology
Endotoxin Level Ultra Low Endotoxin
Host Species Rat
Applications Blocking
Applications FA
Applications WB
€359 - €4,859
Global Shipping: 80+ Countries
White Glove Service: Available upon request
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Distributors: 60+ Countries

Description

system_update_altTechnical Datasheet

Anti-Mouse PD-1 (CD279) [RMP1-14] In Vivo Antibody - Ultra Low Endotoxin

Introducing the Anti-Mouse PD-1 [CD279, RMP1-14] In Vivo Antibody - Ultra Low Endotoxin from Assay Genie, a highly specific monoclonal antibody designed for in vivo applications. This antibody targets the PD-1 (Programmed Cell Death Protein 1), a critical immune checkpoint receptor playing a pivotal role in regulating immune responses, making it ideal for research in immunology, cancer biology, and related fields. With a rat IgG2a isotype, it ensures high purity and ultra-low endotoxin levels (<0.002 EU/µg), perfect for in vivo studies, flow cytometry, functional assays, and other experimental applications. Available in various sizes, it is formulated in a preservative-free phosphate-buffered saline (PBS) solution, ensuring stability and efficacy.

Enhance your research with this reliable and versatile antibody designed to help uncover the intricacies of immune checkpoint pathways and their implications in disease and therapy. PD-1 is a cell surface receptor expressed on T-cells and pro-B cells that plays a significant role in downregulating the immune system by preventing the activation of T-cells, thus promoting self-tolerance and preventing autoimmune diseases. It achieves this through interactions with its ligands, PD-L1 and PD-L2, which are often upregulated in various tumors to evade immune surveillance.

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