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Custom Immunization Schedules


Rockland offers variable immunization schedules and use of different adjuvants on a custom basis and dependent on your need, can extend the collection of production bleeds on a monthly basis post the standard applied schedules show below.

 

 


Rapid Screen Protocol (1 month, 100mL yield from best responder)


Day - 4

Pre-bleed


Day 0

Immunize via an intradermal (ID) route using CFA as adjuvant


Day 7

Booster injection via an intradermal (ID) route using IFA as adjuvant


Day 14

Booster injection via an subcutaneous (SC) route using IFA as adjuvant


Day 28

Booster injection via an subcutaneous (SC) route using IFA as adjuvant


Day 38

Terminal Bleed (Client approved)


Day 38

Ship terminal bleed to client



Fast Protocol (100mL yield from best responder)


Day - 4 

Pre-bleed


Day  0

Immunize via an intradermal (ID) route using CFA as adjuvant


Day  7  

Booster injection via an intradermal (ID) route using IFA as adjuvant


Day 14

Booster injection via a subcutaneous (SC) route using IFA as adjuvant


Day 28 

Booster injection via a subcutaneous (SC) route using IFA as adjuvant 


Day 38 

Test Bleed           


Day 40

Ship pre-immune bleed and test bleed to client


Day 45 

Terminal Bleed (Client approved)


Day 47

Ship terminal bleed to client


Day 49

End of project (Researcher approved)   


Please note that activity after the day 38 test bleed will not be performed without approval by the client (by email or fax).



Standard Protocol (75mL yield per month per best responder)


Day - 4 

Pre-bleed


Day  0  

immunize via an intradermal (ID) route using CFA as adjuvant


Day  7  

Booster injection via an intradermal (ID) route using IFA as adjuvant   


Day 14 

Booster injection via a subcutaneous (SC) route using IFA as adjuvant                   


Day 28 

Booster injection via a subcutaneous (SC) route using IFA as adjuvant


Day 38 

Test Bleed           


Day 40 

Ship pre-immune bleeds and test bleeds to researcher


Day 45 

Production Bleed (Client approved)


Day 52 

Production Bleed (Client approved)       


Day 56 

Booster injection via a subcutaneous (SC) route using IFA as adjuvant                   


Day 66 

Production Bleed (Client approved)


Day 73 

Production Bleed (Client approved)                         


Day 75 

Booster injection via a subcutaneous (SC) route using IFA as adjuvant


Day 85 

Production Bleed (optional – if requested by client - additional charges apply)


Day 92 

Production Bleed (optional – if requested by client - additional charges apply)


Day 94 

Ship production bleeds to client


Day 98 

End of project (Client approved)


Please note that activity after the day 38 test bleed will not be performed without approval by the client (by email or fax).


Dependent on the selected protocol, terminal or production bleeds are collected according to the timelines shown above. Upon conclusion of the applied protocol, you – the researcher – are presented with the option of terminating the project for the collection of a terminal bleed (this only applies to rabbits) or by extending your study for the collection of additional bleeds on a monthly basis.