G5384
Gelatin-Agarose
saline suspension
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About This Item
Productos recomendados
biological source
protein from Porcine skin
Quality Level
form
saline suspension
extent of labeling
≥3 mg per mL
matrix
cross-linked 4% beaded agarose
matrix activation
cyanogen bromide
matrix attachment
amino
matrix spacer
1 atom
storage temp.
2-8°C
Application
Gelatin-Agarose has been used:
- in the isolation of exosomes from human plasma
- to obtain fluorescent labeled enzyme For fluorescence photobleaching recovery (FPR) experiments
- in the purifaction of matrix metalloproteinase-9 by affinity chromatography
Gelatin-agarose is an agarose in saline suspension used for affinity chromatography, protein chromatography and specialty resins. Gelatin-agarose has been used in studies informing pathology-related processes of tissue remodeling as well as sperm-egg interactions in mammals.
Physical form
Suspension in 0.5 M NaCl containing preservative
Storage Class
10 - Combustible liquids
wgk_germany
WGK 3
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Mammalian seminal plasma contains among others, two major families of proteins, namely spermadhesins and those proteins that contain fibronectin type II domains. Spermadhesins are the major proteins of boar and stallion seminal plasma and homologous proteins have been identified in
Journal of immunology (Baltimore, Md. : 1950), 160(9), 4248-4253 (1998-05-09)
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Plasma fibronectin (pFN) cross-linked to fibrin during the injury response provides a provisional matrix required for cells to begin tissue repair. Using a synthetic matrix of pFN and fibrin as a substrate for cell adhesion and spreading, we have determined
Biology of reproduction, 70(3), 656-661 (2003-10-31)
Bovine seminal plasma (BSP) contains a family of major proteins designated BSP-A1/A2, BSP-A3, and BSP-30kDa (collectively called BSP proteins) that bind to sperm at ejaculation and potentiate sperm capacitation. Homologous proteins have been identified in stallion, boar, goat, and ram
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Dipeptidyl peptidase IV (DPP IV) is a cell surface glycoprotein which has been implicated in hepatocyte-extracellular matrix interactions [Hixson, DeLourdes, Ponce, Allison & Walborg (1984) Exp. Cell Res. 152, 402-414; Walborg, Tsuchida, Weeden, Thomas, Barrick, McEntire, Allison & Hixson (1985)
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