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Other Proteins

Recombinant Human NP-1

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Product Details

Catalog Number: 300-42
Description:
Recombinant Human NP-1

Defensins (alpha and beta) are cationic peptides with a broad spectrum of antimicrobial activity that comprise an important arm of the innate immune system.  The α-defensins, which include NP-1, NP-2 and NP-3, are distinguished from the β-defensins by the pairing of their three disulfide bonds.  In addition to antimicrobial activity, NP-1 exhibits chemotactic activity on dendritic cells.  NP-1 is expressed as the C-terminal portion of an inactive precursor protein, which also contains a 19 amino acid N-terminal signal sequence and a 45 amino acid polypeptide.  NP-1 contains a six-cysteine motif that forms three intra-molecular disulfide bonds.  Recombinant Human NP-1 is a 3.4 kDa protein containing 30 amino acid residues.

Source: E.coli

Synonyms: Neutrophil Peptide-1, alpha Defensin-1, HNP-1, Cryptdin

AA Sequence: ACYCRIPACI AGERRYGTCI YQGRLWAFCC

Purity: ≥ 98% by SDS-PAGE gel and HPLC analyses.

Biological Activity: Determined by its ability to chemoattract immature dendritic cells using a concentration of 1.0-10.0 ng/ml.

Calculated Molecular Weight: 3.4 kDa

Accession Number: P59665

Gene ID: 1667

Endotoxin: Endotoxin level is < 0.1 ng/ug of protein (< 1 EU/ug)

Cross Reactivity Cited in References:
Country Of Origin: USA

Not for human use.

Research Interest

Recent Citations

First Author
Wang, Y
Title
Intratumoral expression of mature human neutrophil peptide-1 mediates antitumor immunity in mice.
Citation
Clinical cancer research : an official journal of the American Association for Cancer Research; 15(22) pg6901-11
PubMed ID
First Author
Grigat, J
Title
Chemoattraction of macrophages, T lymphocytes, and mast cells is evolutionarily conserved within the human alpha-defensin family.
Citation
Journal of immunology (Baltimore, Md. : 1950); 179(6) pg3958-65
PubMed ID
First Author
Mount, K L
Title
Haemophilus ducreyi is resistant to human antimicrobial peptides.
Citation
Antimicrobial Agents and Chemotherapy; 51(9) pg3391-3
PubMed ID