8. It is essential to have isotonic conditions, i.e., 300 mosmolar to shield the negative charge on the mucins otherwise anomalously high viscosities will result. 9. It is vital to include controls without enzyme in the mucolysis experiments. Crude mucus samples may contain endogenous pro[r]
1. Introduction Progress in understanding how mucosal surfaces are protected is closely related to the development of morphologic techniques to study the structure and secretory func- tion of the mucosal epithelia. Morphologic methods have allowed characterization of mucus-secreting cells o[r]
An alternative to the radioactive methods is the use of biotinylated mucin sub- strates tagged through either the peptide or carbohydrate moieties of the molecule (6 , 7) . Such assays have been described for protein substrates and adapted for use with microtiter plates (8) . They require s[r]
12. Rentrop, M., Knapp, B., Winter, H., and Schweizer, J. (1986) Aminoalkylsilane-treated slides as support for in situ hybridization of keratin cDNAs to frozen tissue sections under varying fixation and pretreatment condition. Histochem. J. 18, 271–276. 13. Briand, J. P., Muller, S., and Van Re[r]
and Corstedt, I. (1999) Studies on the insoluable glycoprotein complex from human colon: identification of reduction-insensitive MUC2 oligomers and C-terminal cleavage. J. Biol. Chem. 274, 15,828–15,836. 28. Gum, J. R., Hicks, J. W., Toribara, N. W., Siddiki, B., and Kim, Y. S. (1994) Molec[r]
4. Ethidium bromide is not added to DNA before electrophoresis because it is thought to modify the migration of DNA. Acknowledgments The methods described here were developed with the help of Veronique Guyonnet- Duperat (20) and Pascal Pigny (21) . The authors thank Dr. Alexander S. Hill[r]
sodium acetate, pH 4.0); coffee bean α -galactosidase (200 m M Tris-HCl, pH 6.5); bovine testes (100 m M citrate phosphate, pH 4.0). 11. In addition to the colorimetric assays given in this chapter, additional sensitivity can be attained by the use of fluorimetric assays with 4-methyl umbellifer[r]
1. Introduction Northern blot analysis has historically been one of the most common methods used to provide information on the number, length, and relative abundance of mRNAs expressed by a single gene. This technique also generates a record of the total mRNA content expressed by a cell cul[r]
3. Methods 3.1. Preparation of mRNA 1. Total RNA is isolated from cultured cells or human mucosae as described in Chapter 25. In spite of the fact that the purification yield of poly A + mucin fraction is very poor, the purification step of polyA + RNA from total RNA cannot be omitted pri[r]
TRANG 12 BROCKHAUSEN TABLE 1 MUCIN GLYCOSYLTRANSFERASES, THEIR SUBSTRATES AND PRODUCTS, AND HPLC CONDITIONS FOR PRODUCT ISOLATION HPLC Path Enzyme Substrate Product column % AN a Polypep[r]
3. Methods 3.1. Cell Culture in the Presence of GalNAc α -O-benzyl 3.1.1. Conditions of Use of GalNAc α -O-benzyl GalNAc α - O -benzyl is directly dissolved in the culture medium for 2 h at room temperature with continuous stirring. Then, the medium is sterilized by filtration. GalNAc α[r]
5. Monitor the eluate on-line with a UV monitor and collect fractions using a fraction col- lector and subject to the appropriate carbohydrate and antibody analyses. 3.6. Analysis of Mucins Methods for the detection and analysis of mucins are dealt with in other chapters in this volume. H[r]
In this Chapter, we focus on the identification of each of the known MUC-type mucin precursors by immunoprecipitation using antipeptide antibodies. Moreover, a number of biochemical and cell biological assays will be described which establish the presence in the RER of each alleged MUC-type mucin pr[r]
MUC1/neo-positive population of cells sorted by flow cytometry died within 2 wk with- out proliferation. Cloning of MUC1/neo-positive cells by limiting dilution in a 96-well plate resulted in progressive death of these cells, whereas neo-positive only cells expanded. We do not have a good explanat[r]
8. Horseradish peroxidase-labeled rabbit antihuman IgG and IgM, both from Dako A/S, Glostrup, Denmark. Dilute the conjugate 1:10,000 in phosphate/salt buffer containing 0.5% BSA. 9. Substrate solution containing 0.06 mg/mL of tetramethylbenzidine (TMB) diluted in 0.1 M sodium acetate/citric[r]
3. Transfer the marrow into a 20-mL universal. Allow any fragments of bone or muscle to fall to the bottom of the tube under gravity and the transfer the supernatant to a fresh universal. 4. Count cells and resuspend at 3.33 × 10 5 /mL in IMDM ( see Subheading 2., item 1e ) plus 5%FCS and mouse GM-[r]
In addition to the MHC-unrestricted CTLs, some MUC1-specific MHC-restricted CTLs have also been identified. Patients who are HLA-A11 and HLA-A3 have CTLs that recognize a nine amino acid peptide from the tandem repeat region bound to these alleles (6) . Another peptide has been reported that binds H[r]
T.L đi, đứng, bị, lẫy theo cữ và cịn hơi nhanh hơn so với các trẻ khác. Được 2 tháng tuổi cháu đã biết lẫy, 9 tháng tuổi cháu đã biết đi tốt và biết nĩi khoảng 5 từ. Gọi “T.L ơi” cháu biết “ dạ” rất rõ ràng. Hỏi cháu cĩ ăn đồ gì đĩ khơng cháu biết nĩi “ khơng ” hoặc “ cĩ”. Khi xem phim[r]
Methods outlined for the isolation of bacteria from the rectal mucosa are essentially destructive, and primarily provide details of the types and numbers of different species that take part in this process. They do not contribute information concerning the mul- ticellular organization of biof[r]
2. Wash wells 24 times with PBS. 3. Block for 2 h at room temperature (or overnight at 4 ° C) by adding 200 µ L of 1% BSA/ PBS to each well. 4. After blocking, wash wells twice with PBS/Tween and incubate with 100 µ L of 5 µ g/mL biotinylated wheat germ agglutinin (WGA) for 45 min at room tem[r]