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Ch 8.Immunohistoch / immunology
Ch 10.GC/MS, NMR and Proteomics
Biochemistry (Chapters and Vocabulary) -unit 1-50, 51-100, 101-150, 151-200, 201-250, 251-300, 301-350, 351-400, 401-450, 451-500
103: Coreceptor CD4.
105: Presentation of Peptides from Internalized Proteins.
106: Consequences of Cytotoxic-T-Cell Action.
107: T-Cell Activation.
109: The Coreceptor CD8.
110: T-Cell Receptor Class I MHC Complex.
111: T-Cell Receptor.
112: Anchor Residues.
113: Class I MHC Peptide-Binding Site.
114: Class I MHC Protein.
115: Presentation of Peptides from Cytosolic Proteins.
117: The Discovery of Catalytic RNA Was Revealing in Regard to Both Mechanism and Evolution
118: Complex Formed by TATA-Box-Binding Protein and DNA.
119: Transcription
Initiation.
120: CAAT Box and GC Box.
121: TATA Box.
123: Eukaryotic RNA polymerases
124: Transcription and Translation.
125: Transcription Is Catalyzed by RNA Polymerase
126: Antibiotic Action.
127: Primary Transcript.
128: Mechanism For the Termination of Transcription by Rho Protein.
129: Effect
of Rho Protein On the Size of RNA Transcripts.
130: Termination Signal.
131: RNA-DNA Hybrid Separation.
133: DNA Unwinding.
134: Alternative Promoter Sequences.
135: Structure of the Sigma Subunit.
136: Prokaryotic Promoter Sequences.
137: Footprinting.
138: RNA Polymerase Active Site.
139: Subunits of RNA polymerase from E. coli
140: RNA synthesis is a key step in the expression of genetic information.
141: RNA Polymerase Structures.
142: An Overview of RNA Synthesis
143: RNA Synthesis and Splicing
144: Problems
145: Summary
146: Comparison of Splicing Pathways.
148: Structure of a Self-Splicing Intron.
149: Self-Splicing.
150: The Transcription Products of All Three Eukaryotic Polymerases Are Processed