Identification and Amplification of a Novel Egg Case Silk Gene In Latrodectus hesperus

Poster Number

15

Format

Poster Presentation

Abstract/Artist Statement

Spider silks are characteristically strong and elastic. The potential of using spider silk for various industrial applications is enormous once mass production of spider silk becomes possible. Made by seven different glands of certain orb-weaving spiders, multiple types of silk are produced with unique chemical and mechanical properties. The seven glands are the major ampullate, minor ampullate, flagelliform, pyriform, aciniform, aggregate, and tubuliform glands. In this experiment, degenerate oligonucleotides were designed based on the peptide fragments obtained from tryptic digestion of Strong-1, a large molecular weight protein identified to be a major component of Latrodectus hesperus egg case silk. We are currently screening a cDNA library using polymerase chain reaction (PCR) to amplify pieces of the gene corresponding to Strong-1. Results will be discussed.

Location

Callison Hall

Start Date

6-5-2006 10:00 AM

End Date

6-5-2006 12:00 PM

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May 6th, 10:00 AM May 6th, 12:00 PM

Identification and Amplification of a Novel Egg Case Silk Gene In Latrodectus hesperus

Callison Hall

Spider silks are characteristically strong and elastic. The potential of using spider silk for various industrial applications is enormous once mass production of spider silk becomes possible. Made by seven different glands of certain orb-weaving spiders, multiple types of silk are produced with unique chemical and mechanical properties. The seven glands are the major ampullate, minor ampullate, flagelliform, pyriform, aciniform, aggregate, and tubuliform glands. In this experiment, degenerate oligonucleotides were designed based on the peptide fragments obtained from tryptic digestion of Strong-1, a large molecular weight protein identified to be a major component of Latrodectus hesperus egg case silk. We are currently screening a cDNA library using polymerase chain reaction (PCR) to amplify pieces of the gene corresponding to Strong-1. Results will be discussed.