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Recombinant Human Lipocalin-2/NGAL Protein, CF  50 UG图1

Recombinant Human Lipocalin-2/NGAL Protein, CF 50 UG

2024-11-24 18:20IP属地 广东省东莞市 电信00留言

1757-LC

 

Formulation Supplied as a 0.2 μm filtered solution in MES and NaCl.





Shipping The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below.


Stability & Storage:       Use a manual defrost freezer and avoid repeated freeze-thaw cycles.      

  • 6 months from date of receipt, -20 to -70 °C as supplied.

  • 3 months, -20 to -70 °C under sterile conditions after opening.


Assay Procedure

Materials

    1. Prepare a curve of Fe3+ in deionized water with the following serial dilutions: 640, 320, 160, 80, 40, 20, 10, 5, and 2.5 µM.

    2. Prepare 1 mM DHBA in Ligand Buffer from powder stock.

    3. Combine equal volumes of the Fe3+ curve with 1 mM DHBA. Include a control containing 1 mM DHBA and Ligand Buffer.

    4. Incubate at room temperature for 10 minutes. A curve of the metal ligand complex of Fe(DHBA)3 is formed.

    5. After incubation, perform 5 fold dilutions to the curve using Assay Buffer.

    6. Dilute rhLipocalin-2 (MW: 21905 Da) to 4 µM in Assay Buffer.

    7. In the plate, load 50 µL of the diluted Fe(DHBA)3 complex curve and 50 µL of 4 µM rhLipocalin-2.

    8. Incubate at room temperature for 30 minutes.

    9. Read at excitation and emission wavelengths of 280 nM and 340 nM, respectively in endpoint mode.

    10. Plot a 4-parameter curve of Fe(DHBA)3 concentration (x-axis) versus RFUs (y-axis), and calculate a BC50 from the curve.

Per Well:

Background: Lipocalin-2/NGAL

Members of Lipocalin family share a highly conserved fold with an eight-stranded antiparallel beta barrel, and act as a transporters, carrying small molecules to specific cells (1). Lipocalin-2, also known as Neutrophil Gelatinase-Associated Lipocalin (NGAL), was originally identified as a component of neutrophil granules (2). It is a 25 kDa protein existing in monomeric and homo- and heterodimeric forms, the latter as a dimer with human neutrophil gelatinases (MMP-9) (2). Its expression has been observed in most tissues normally exposed to microorganism, and its synthesis is induced in epithelial cells during inflammation (3). Lipocalin-2 has been implicated in a variety of processes including cell differentiation, tumorigenesis, and apoptosis (3‑5). Studies indicate that Lipocalin-2 binds a bacterial catecholate sidropore bound to ferric ion such as enterobactin with a subnanomolar dissociation constant (Kd = 0.41 nM) (6). The bound ferric enterobactin complex breaks down slowly in a month into dihydroxybenzoyl serine and dihydroxybenzoic acid (DHBA). It also binds to a ferric DHBA complex with much less Kd values (7.9 nM) (6). Secretion of Lipocalin‑2 in immune cells increases by stimulation of Toll-like receptor as an acute phase response to infection. As a result, it acts as a potent bacteriostatic reagent by sequestering iron (7). Moreover, Lipocalin-2 can alter the invasive and metastatic behavior of Ras-transformed breast cancer cells in vitro and in vivo by reversing epithelial to mesenchymal transition inducing activity of Ras, through restoration of E-cadherin expression, via effects on the Ras-MAPK signaling pathway (8).

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