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Serum albumin

Manufactured by R&D Systems
Sourced in Germany

Serum albumin is a purified protein derived from human blood plasma. It functions as a transport and regulatory protein, helping to maintain fluid balance and pH levels in the body.

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3 protocols using serum albumin

1

Cochlear Implant Drug Delivery

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The device (Cochlear Ltd., Sydney, Australia) consisted of six platinum contacts, 0.3 mm each, with 0.4 mm spacing (Figure 2). Beginning on the electrode tip, only the first and fourth contacts were linked to the connector via parylene-insulated platinum–iridium wires. The wires were embedded in a silicone matrix of about 450 µm outer diameter. The silicone matrix included a drug delivery channel (diameter: ~200 µm) with a single opening at the electrode tip. Wires and the drug channel separated in a distance of 22 mm from the tip (Figure 2A). During surgery, the silicone tube for drug delivery was connected to the flow moderator of a mini-osmotic pump with an infusion rate of 0.5 µL/h, suitable for 14 days delivery (Alzet model 2002; Durect Corp., Cupertino, CA, USA). The day before surgery, the pumps were either filled with AP with addition of 0.1% guinea pig serum albumin (Sigma-Aldrich, Steinheim, Germany) [19 (link)] or 50 ng BDNF (R&D Systems, Wiesbaden, Germany) diluted in 1 mL of serum albumin containing AP and primed in saline at 37 °C overnight.
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2

Immunohistochemical Analysis of Lung Tissue

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Following blocking, sections were incubated with primary antibodies against laminin (1:200, Sigma), serum albumin (1:300, R&D systems), collagen (1:500, R&D systems), IL-33 (1:200, R&D systems) and siglec-F (1:200, BD Biosciences) diluted in blocking buffer at RT. To detect the tdTomato in Red5 mice, mice were incubated with antibodies against DsRed (1:200, Takara) for 3 hours at RT. Cross-sections were then washed in 1X PBS and incubated with corresponding secondary antibodies to detect the antigen of interest.
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3

Immunohistochemical Analysis of Lung Tissue

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Following blocking, sections were incubated with primary antibodies against laminin (1:200, Sigma), serum albumin (1:300, R&D systems), collagen (1:500, R&D systems), IL-33 (1:200, R&D systems) and siglec-F (1:200, BD Biosciences) diluted in blocking buffer at RT. To detect the tdTomato in Red5 mice, mice were incubated with antibodies against DsRed (1:200, Takara) for 3 hours at RT. Cross-sections were then washed in 1X PBS and incubated with corresponding secondary antibodies to detect the antigen of interest.
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