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HAP stands for “High Affinity Purification”; it is a patented, novel purification method for custom oligos developed by Bio Basic. After synthesis the DMT-ON-oligo in the crude oligo mixture is selectively absorbed on a high affinity resin within a HAP column, this allows incomplete oligo fragments pass through while keeping majority of the full length oligos. The full length oligo is retrieved by removing the DMT protection group under mild acid conditions.

The HAP process provides two major advantages, higher purity, superior to that of the De-Salted method (purity of a standard 20 bases-HAP is >85%, 30 bases-HAP > 80% etc.), and lower cost compared to PAGE or HPLC methods.

O.D. stands for Optical Density units; it is based on absorbance readings at 260nm. For synthesis facilities that use phosphoramidite synthesis, O.D. measurements are a means to quantify the amount of available oligo after purification i.e. the FINAL YIELD of the oligo. As a rough estimate 1 O.D. ~ 33 ug. When comparing oligo synthesis services, the O.D. should be compared (the final yield) and not the initial synthesis scale (in “nmol”) which is the quantity of the starting material required before synthesis of the oligo. From this, the final “nmol” yield will vary on the length, sequence and molecular weight of the individual oligo.

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HAP stands for “High Affinity Purification”; it is a patented, novel purification method for custom oligos developed by Bio Basic. After synthesis the DMT-ON-oligo in the crude oligo mixture is selectively absorbed on a high affinity resin within a HAP column, this allows incomplete oligo fragments pass through while keeping majority of the full length oligos. The full length oligo is retrieved by removing the DMT protection group under mild acid conditions.

The HAP process provides two major advantages, higher purity, superior to that of the De-Salted method (purity of a standard 20 bases-HAP is >85%, 30 bases-HAP > 80% etc.), and lower cost compared to PAGE or HPLC methods.

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HAP stands for “High Affinity Purification”; it is a patented, novel purification method for custom oligos developed by Bio Basic. After synthesis the DMT-ON-oligo in the crude oligo mixture is selectively absorbed on a high affinity resin within a HAP column, this allows incomplete oligo fragments pass through while keeping majority of the full length oligos. The full length oligo is retrieved by removing the DMT protection group under mild acid conditions.

The HAP process provides two major advantages, higher purity, superior to that of the De-Salted method (purity of a standard 20 bases-HAP is >85%, 30 bases-HAP > 80% etc.), and lower cost compared to PAGE or HPLC methods.

O.D. stands for Optical Density units; it is based on absorbance readings at 260nm. For synthesis facilities that use phosphoramidite synthesis, O.D. measurements are a means to quantify the amount of available oligo after purification i.e. the FINAL YIELD of the oligo. As a rough estimate 1 O.D. ~ 33 ug. When comparing oligo synthesis services, the O.D. should be compared (the final yield) and not the initial synthesis scale (in “nmol”) which is the quantity of the starting material required before synthesis of the oligo. From this, the final “nmol” yield will vary on the length, sequence and molecular weight of the individual oligo.
O.D. stands for Optical Density units; it is based on absorbance readings at 260nm. For synthesis facilities that use phosphoramidite synthesis, O.D. measurements are a means to quantify the amount of available oligo after purification i.e. the FINAL YIELD of the oligo. As a rough estimate 1 O.D. ~ 33 ug. When comparing oligo synthesis services, the O.D. should be compared (the final yield) and not the initial synthesis scale (in “nmol”) which is the quantity of the starting material required before synthesis of the oligo. From this, the final “nmol” yield will vary on the length, sequence and molecular weight of the individual oligo.
O.D. stands for Optical Density units; it is based on absorbance readings at 260nm. For synthesis facilities that use phosphoramidite synthesis, O.D. measurements are a means to quantify the amount of available oligo after purification i.e. the FINAL YIELD of the oligo. As a rough estimate 1 O.D. ~ 33 ug. When comparing oligo synthesis services, the O.D. should be compared (the final yield) and not the initial synthesis scale (in “nmol”) which is the quantity of the starting material required before synthesis of the oligo. From this, the final “nmol” yield will vary on the length, sequence and molecular weight of the individual oligo.
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