G0411
Prionex® Highly purified Type A
aqueous solution
Sinónimos:
Gelatin, Prionex® Highly purified Type A
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About This Item
Productos recomendados
biological source
Porcine bone
Quality Level
sterility
aseptically processed
form
aqueous solution
technique(s)
ELISA: suitable
microbiological culture: suitable
western blot: suitable
General description
Gelatin is a heterogeneous mixture of water-soluble proteins of high average molecular masses, present in collagen. The proteins are extracted by boiling skin, tendons, ligaments, bones, etc. in water. Type-A gelatin is derived from acid-cured (acid-hydrolyzed) tissue. Type-B gelatin is derived from lime-cured (base/alkaline-hydrolyzed) tissue. Gelatin is a biocompatible polymer.
Application
Prionex® Highly purified Type A has been used:
- for coating cell culture to improve attachment of cells, and was added to polymerase chain reaction (PCR) to help stabilize Taq DNA
- as a blocking reagent in Western blotting, enzyme linked immunosorbent assay (ELISA), and immunohistochemistry
- as a component of media for species differentiation in bacteriology
- as a delivery vehicle for the release of bioactive molecules and in the generation of scaffolds for engineering applications
- in the murine lethality assay which is used to examine the ability of SMAbs to neutralize the effects of BoNT/A1 in vivo
Legal Information
Prionex is a registered trademark of Pentapharm AG, Basel
Storage Class
11 - Combustible Solids
wgk_germany
nwg
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Certificados de análisis (COA)
Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»
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We tested instantized dry milk, casein, gelatins from pig and fish skin, serum albumin and several other proteins for their abilities to block non-specific binding (NSB) of a peroxidase-conjugated immunoglobulin to polystyrene microtiter plate wells. Each blocking protein was tested
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