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Biomaterials

Chicken Serum Sterile

Product Sizes
500 ml
£1741.00
D102-00-0500-500ML
About this Product
SKU:
D102-00-0500
Additional Names:
Chicken serum for cell culture, cell culture grade chicken serum, sterile serum from chicken
Application:
Immunohistochemistry
Buffer:
None
CE/IVD:
RUO
Concentration:
80 mg/ml
Extra Details:
Chicken Serum is used as a supplement to cell culture media. Chicken Serum provides a broad spectrum of macromolecules, carrier proteins for lipoid substances and trace elements, attachment and spreading factors, low molecular weight nutrients, and hormones and growth factors that promote cell growth and health. Be certain to maintain Good Cell Culture Practice, and maintain sterility of cultures that require media supplementation. Chicken Serum is ideal for investigators in Cancer and Cell Biology.
Physical State:
Liquid
Shipping Conditions:
Dry Ice
Specificity:
Chicken Serum was prepared by removal of fibrinogen through clot formation. Chicken Serum was separated from cellular components and purified through centrifugation and filtration techniques. Assay by immunoelectrophoresis resulted in multiple precipitin arcs against anti-Chicken Serum. Chicken Serum was sterilized using a 0.22 micron filter and found to be negative for bacterial growth after incu
Storage Conditions:
-20[o]C Avoid freeze/thaw cycles.
Supplier:
Rockland Inc
Type:
Biomaterials: Blood Products
Chicken Serum is used as a supplement to cell culture media. Chicken Serum provides a broad spectrum of macromolecules, carrier proteins for lipoid substances and trace elements, attachment and spreading factors, low molecular weight nutrients, and hormones and growth factors that promote cell growth and health. Chicken Serum was prepared by removal of fibrinogen through clot formation. Chicken Serum was separated from cellular components and purified through centrifugation and filtration techniques.
Intranasal infection with HSV-1 induces blood leukocytes infiltration in the CNS of chimeric C57BL/6 mice. Representative micrographs illustrating the localization of GFP+ infiltrating cells in the olfactory bulb, the interbrain and the hindbrain of GFP+/- to WT mice. Sixteen week-old chimeric mice were infected with HSV-1 by the intranasal route and sacrificed prior to (negative control) and on days 4, 6, 8 and 10 post-infection (5 mice per group). Free-floating sections were washed 3 times for 15 min in potassium PBS (KPBS) and incubated for 30 min in KPBS containing 4% goat or chicken (p/n D102-00-0050) serum, 1% BSA and 0.4% Triton X-100. (A) Brain slices of 25-um thick were processed for immunohistochemistry staining with a primary polyclonal goat anti-GFP and a secondary Alexa 488-conjugated chicken anti-goat antibodies (green). In non-infected mice (NI), no GFP+ cells could be found in the brain parenchyma. Following infection, peripheral leukocytes infiltrated the CNS and could be detectable mainly in the olfactory bulb, the interbrain and the hindbrain. Scale bar 100 um. Fig 3. PMID: 26700486.