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Official Technical Resources & 
SOP Manuals (v2026.01)


Access complete handling guidelines, experimental protocols (in vitro and in vivo), BSA dose conversion matrices, and analytical reference profiles—formatted into a print-ready PDF for your laboratory binder.

Updated for 2026 • Optimized for Standard A4 & Letter Printing • ISO-Aligned SOPs


Official Technical Resources & SO Manuals (v2026.01)


Access complete handling guidelines, experimental protocols (in vitro and in vivo), BSA dose conversion matrices, and analytical reference profiles—formatted into a print-ready PDF for your laboratory binder


Download Complete Manual (PDF)

Updated for 2026 • Optimized for Standard A4 & Letter Printing • ISO-Aligned SOPs

Technical Downloads


Reference Standard Technical Manual & Laboratory Handling Guidebook 

English | PDF | 8.9 MB

Download


Manual Teknis Bahan Acuan & Panduan Penanganan Laboratorium 

Indonesian | PDF | 9.7 MB

Download


Notice & Intended Use: All technical documentation, protocols, and manuals provided by MarkHerb are intended strictly for scientific research and laboratory use. Products are not intended for human therapeutic, diagnostic, or clinical applications.

Technical Downloads:


Document Title

Format

File Size

Language

Quick Link


Reference Standard Technical Manual &

LaboratoryHandling Guidebook

PDF

8.5 MB

English

Download 

Manual Teknis Bahan Acuan & Panduan Penanganan Laboratorium

PDF

8.9 MB

Indonesian

Download

Updated for 2026 • Optimized for Standard A4 & Letter Printing • ISO-Aligned SOPs


Notice & Intended Use: All technical documentation, protocols, and manuals provided by MarkHerb are intended strictly for scientific research and laboratory use. Products are not intended for human therapeutic, diagnostic, or clinical applications.

What's Inside The Manual? 

(Content Overview)


Unboxing & Consolidating Micro-Quantities

This section outlines standard operating procedures for receiving and unboxing powder and liquid compounds. It provides step-by-step guidance on gentle tapping and micro-centrifugation (200–500 RPM) to ensure low-volume liquid droplets and fine powders consolidate fully at the base of the vial prior to seal break, minimizing product loss.


Storage & Stability Benchmark Matrix

Learn how to maintain compound integrity and prevent degradation over time. This section establishes thermal storage thresholds across 2–8 °C, -20 °C, and -80 °C for both dry powders and liquid stock solutions, while emphasizing single-use aliquoting strategies to eliminate harmful freeze-thaw cycles.


Analytical Solution Preparation SOP

Designed for high-precision analytical workflows, this module details micro-weighing protocols down to (0.01 mg) alongside strict tare drying guidelines (115 °C). It also provides comprehensive solubilization routines for poorly soluble compounds using organic solvents such as MeOH, MeCN, DCM, CHCl3, and THF.


Cell-Based & Enzyme Bioassay Workflows

Ensure cell viability and accurate bioassay results with safe co-solvent handling procedures. This section details stepwise dilution techniques that prevent localized precipitation while keeping final DMSO concentrations below < 0.5%  v/v. It includes standardized molarity formulas to simplify working solution calculations:

  

In Vivo Formulation & Interspecies Dose Conversion

Translate experimental dosages accurately across animal species using FDA-aligned Body Surface Area (BSA) normalization factors (Km). This guide presents three distinct vehicle formulation schemes—co-solvent mixtures, SBE-β-CD inclusion complexes, and lipophilic oils, alongside the interspecies dose translation formula:

  

Thin-Layer Chromatography (TLC) & Solvent Miscibility

Verify compound identity and optimize mobile phase design with practical TLC instructions. This section covers plate preparation with a 4.0 cm elution path, UV 254 nm / 366 nm visualization protocols, Rf retention calculations, and a comprehensive solvent miscibility guide to prevent phase separation during analytical testing.

What's Inside The Manual? 

(Content Overview)


Unboxing & Consolidating Micro-Quantities

This section outlines standard operating procedures for receiving and unboxing powder and liquid compounds. It provides step-by-step guidance on gentle tapping and micro-centrifugation (200–500 RPM) to ensure low-volume liquid droplets and fine powders consolidate fully at the base of the vial prior to seal break, minimizing product loss.


Storage & Stability Benchmark Matrix

Learn how to maintain compound integrity and prevent degradation over time. This section establishes thermal storage thresholds across 2–8 °C, -20 °C, and -80 °C for both dry powders and liquid stock solutions, while emphasizing single-use aliquoting strategies to eliminate harmful freeze-thaw cycles.


Analytical Solution Preparation SOP

Designed for high-precision analytical workflows, this module details micro-weighing protocols down to (0.01 mg) alongside strict tare drying guidelines (115 °C). It also provides comprehensive solubilization routines for poorly soluble compounds using organic solvents such as MeOH, MeCN, DCM, CHCl3, and THF.


Cell-Based & Enzyme Bioassay Workflows

Ensure cell viability and accurate bioassay results with safe co-solvent handling procedures. This section details stepwise dilution techniques that prevent localized precipitation while keeping final DMSO concentrations below < 0.5%  v/v. It includes standardized molarity formulas to simplify working solution calculations:

  


In Vivo Formulation & Interspecies Dose Conversion

Translate experimental dosages accurately across animal species using FDA-aligned Body Surface Area (BSA) normalization factors (Km). This guide presents three distinct vehicle formulation schemes—co-solvent mixtures, SBE-β-CD inclusion complexes, and lipophilic oils, alongside the interspecies dose translation formula:

  


Thin-Layer Chromatography (TLC) & Solvent Miscibility

Verify compound identity and optimize mobile phase design with practical TLC instructions. This section covers plate preparation with a 4.0 cm elution path, UV 254 nm / 366 nm visualization protocols, Rf retention calculations, and a comprehensive solvent miscibility guide to prevent phase separation during analytical testing.




Ready to Elevate Your Research or Product Formulation?


Speak directly with our phytochemical experts to request reference compound catalog quotes, custom isolation projects, or chromatography media testing.

Explore Our Products



Ready to Elevate Your Research or Product Formulation?


Speak directly with our phytochemical experts to request reference compound catalog quotes, custom isolation projects, or chromatography media testing.


Explore Our Products