60K-PXBK38, HCYTA-60K-PX48, HCYTMAG-60K-PXBK48
Control Catalog # HCYTA-6060-1 Lot # A60MG-103 and A60MG-203
***Additional Analytes on reverse side***
Note: The Quality Control Ranges are generated with
viable cells (V)
using the formula:
V = (AN – AD) × 10 × 104 × 0.5 mL
Cell count per mL = Average cell count per square ×
Dilution factor × 104
Day 0 – Plating Cells
1. Adjust
viable cells (V)
using the formula:
V = (AN – AD) × 10 × 104 × 0.5 mL
Cell count per mL = Average cell count per square ×
Dilution factor × 104
Day 0 – Plating Cells
1. Adjust
viable cells (V)
using the formula:
V = (AN – AD) × 10 × 104 × 0.5 mL
Cell count per mL = Average cell count per square ×
Dilution factor × 104
Day 0 – Plating Cells
1. Adjust
.
6. Determine if enzymatic treatment (unmasking) of
the antigen is required prior to application of the
primary antibody.
References
1. Arnold, S.J. et al., Dev. Biol., 296(1), 104-118
(
viable cells (V)
using the formula:
V = (AN – AD) × 10 × 104 × 0.5 mL
Cell count per mL = Average cell count per square ×
Dilution factor × 104
Day 0 – Plating Cells
1. Adjust
viable cells (V)
using the formula:
V = (AN – AD) × 10 × 104 × 0.5 mL
Cell count per mL = Average cell count per square ×
Dilution factor × 104
Day 0 – Plating Cells
1. Adjust
viable cells (V)
using the formula:
V = (AN – AD) × 10 × 104 × 0.5 mL
Cell count per mL = Average cell count per square ×
Dilution factor × 104
Day 0 – Plating Cells
1. Adjust
viable cells (V)
using the formula:
V = (AN – AD) × 10 × 104 × 0.5 mL
Cell count per mL = Average cell count per square ×
Dilution factor × 104
Day 0 – Plating Cells
1. Adjust
viable cells (V)
using the formula:
V = (AN – AD) × 10 × 104 × 0.5 mL
Cell count per mL = Average cell count per square ×
Dilution factor × 104
Day 0 – Plating Cells
1. Adjust
viable cells (V)
using the formula:
V = (AN – AD) × 10 × 104 × 0.5 mL
Cell count per mL = Average cell count per square ×
Dilution factor × 104
Day 0 – Plating Cells
1. Adjust
viable cells (V)
using the formula:
V = (AN – AD) × 10 × 104 × 0.5 mL
Cell count per mL = Average cell count per square ×
Dilution factor × 104
Day 0 – Plating Cells
1. Adjust
viable cells (V)
using the formula:
V = (AN – AD) × 10 × 104 × 0.5 mL
Cell count per mL = Average cell count per square ×
Dilution factor × 104
Day 0 – Plating Cells
1. Adjust
viable cells (V)
using the formula:
V = (AN – AD) × 10 × 104 × 0.5 mL
Cell count per mL = Average cell count per square ×
Dilution factor × 104
Day 0 – Plating Cells
1. Adjust
viable cells (V)
using the formula:
V = (AN – AD) × 10 × 104 × 0.5 mL
Cell count per mL = Average cell count per square ×
Dilution factor × 104
Day 0 – Plating Cells
1. Adjust
viable cells (V)
using the formula:
V = (AN – AD) × 10 × 104 × 0.5 mL
Cell count per mL = Average cell count per square ×
Dilution factor × 104
Day 0 – Plating Cells
1. Adjust
viable cells (V)
using the formula:
V = (AN – AD) × 10 × 104 × 0.5 mL
Cell count per mL = Average cell count per square ×
Dilution factor × 104
Day 0 – Plating Cells
1. Adjust
viable cells (V)
using the formula:
V = (AN – AD) × 10 × 104 × 0.5 mL
Cell count per mL = Average cell count per square ×
Dilution factor × 104
Day 0 – Plating Cells
1. Adjust
viable cells (V)
using the formula:
V = (AN – AD) × 10 × 104 × 0.5 mL
Cell count per mL = Average cell count per square ×
Dilution factor × 104
Day 0 – Plating Cells
1. Adjust
viable cells (V)
using the formula:
V = (AN – AD) × 10 × 104 × 0.5 mL
Cell count per mL = Average cell count per square ×
Dilution factor × 104
Day 0 – Plating Cells
1. Adjust
viable cells (V)
using the formula:
V = (AN – AD) × 10 × 104 × 0.5 mL
Cell count per mL = Average cell count per square ×
Dilution factor × 104
Day 0 – Plating Cells
1. Adjust
viable cells (V)
using the formula:
V = (AN – AD) × 10 × 104 × 0.5 mL
Cell count per mL = Average cell count per square ×
Dilution factor × 104
Day 0 – Plating Cells
1. Adjust
Labeling of Eschericahia coli Ribosomes with an Aryl Azide Analog of Puromycin. FEBS Lett.
1978, 90, 203.
33 Nomoto, S.; Shiba, T. Synthesis of Nß-Methyl-l-arginine, a Component Amino Acid in a New Antibiotic