1703930/170-3930:Mini Trans-Blot Electrophoretic Transfer Cell, includes 2 gel holder cassettes, 4 foam pads, modular electrode assembly, blue cooling unit, lower buffer tank, lid with cables
1703935/170-3935:Mini Trans-Blot Module, without lower buffer tank and lid
1703931/170-3931:Mini Gel Holder Cassette黑色转印夹
1703933/170-3933:Foam Pads, 8 x 11 cm, 4PK,海绵垫
1703932/170-3932:转印滤纸Thick Blot Paper, 7.5 x 10 cm, for Mini Trans-Blot cassette, 50张/包
1703812/170-3812:Mini Trans-Blot Central Core,转印内芯(红黑模块)
Bio-Rad伯乐快速蛋白测定血清蛋白标准品5000207 500-0207,Quick Start Bovine Serum Albumin(BSA) Standard Set.Pkg of 2, set of 7 protein concentrations standards, 0.125–2.0 mg/ml, for use with Quick Start Bradford。
Bio-Rad伯乐快速蛋白测定血清蛋白标准品5000207 500-0207
Quick Start Bovine Serum Albumin(BSA) Standard Set.Pkg of 2, set of 7 protein concentrations standards, 0.125–2.0 mg/ml, for use with Quick Start Bradford。
1658001/165-8001:小型垂直电泳槽 10-well, 1.0 mm thickness; 4-gel system includes 5 combs, 1 set of glass plates (5 short plates and 5 spacer plates), 2 casting stands, 4 casting frames, sample loading guide, electrode assembly, companion running module, tank, lid with power cables, mini cell buffer dam
1658000/165-8000:小型垂直电泳槽, 10-well, 0.75 mm thickness; 4-gel system includes 5 combs, 1 set of glass plates (5 short plates and 5 spacer plates), 2 casting stands, 4 casting frames, sample loading guide, electrode assembly, companion running module, tank, lid with power cables, mini cell buffer dam
1658002/165-8002:小型垂直电泳槽, 10-well, 0.75 mm thickness; 2-gel system includes 5 combs, 1 set of glass plates (5 short plates and 5 spacer plates), casting stand, 2 casting frames, sample loading guide, electrode assembly, tank, lid with power cables, mini cell buffer dam
1658003/165-8003:小型垂直电泳槽, 10-well, 1.0 mm thickness; 2-gel system includes 5 combs, 1 set of glass plates (5 short plates and 5 spacer plates), casting stand, 2 casting frames, sample loading guide, electrode assembly, tank, lid with power cables, mini cell buffer dam
1658004/165-8004:小型垂直电泳槽for Mini Precast Gels, 4-gel system includes electrode assembly, companion running module, tank, lid with power cables, mini cell buffer dam
1658005/165-8005:小型垂直电泳槽 for Mini Precast Gels, 2-gel system includes electrode assembly, tank, lid with power cables, mini cell buffer dam
1658006/165-8006:小型垂直电泳槽10-well, 1.5 mm thickness; 4-gel system includes 5 combs, 1 set of glass plates (5 short plates and 5 spacer plates), 2 casting stands, 4 casting frames, sample loading guide, electrode assembly, companion running module, tank, lid with power cables, mini cell buffer dam
1658006/165-8007:小型垂直电泳槽, 10-well, 1.5 mm thickness; 2-gel system includes 5 combs, 1 set of glass plates (5 short plates and 5 spacer plates), casting stand, 2 casting frames, sample loading guide, electrode assembly, tank, lid with power cables, mini cell buffer dam
1658025/165-8025:小型垂直电泳槽系统Mini-PROTEAN Tetra Cell and PowerPac Basic Power Supply, includes #165-8001 and #164-5050
1658026/165-8026:小型垂直电泳槽系统Mini-PROTEAN Tetra Cell and PowerPac Universal Power Supply, includes #165-8001 and #164-5070
1658027/165-8027:小型垂直电泳槽系统Mini-PROTEAN Tetra Cell and PowerPac HC Power Supply, includes #165-8001 and #164-5052
1658028/165-8028:小型垂直电泳槽系统Mini-PROTEAN Tetra Cell and PowerPac HV Power Supply, includes #165-8001 and #164-5056
1658029/165-8029:小型垂直电泳槽系统Mini-PROTEAN Tetra Cell and Mini Trans-Blot Module, includes #165-8001 and #170-3935
1658030/165-8030:小型垂直电泳槽系统Mini-PROTEAN Tetra Cell for Mini Precast Gels and Mini Trans-Blot Module, includes #165-8004 and #170-3935
1658033/165-8033:小型垂直电泳槽系统Mini-PROTEAN Tetra Cell, Mini Trans-Blot Module, and PowerPac Basic Power Supply, includes #165-8001, #170-3935, and #164-5050
1658034/165-8034:小型垂直电泳槽系统Mini-PROTEAN Tetra Cell for Mini Precast Gels, Mini Trans-Blot Module, and PowerPac Basic Power Supply, includes #165-8004, #170-3935, and #164-5050
1658035/165-8035:小型垂直电泳槽系统Mini-PROTEAN Tetra Cell, Mini Trans-Blot Module, and PowerPac HC Power Supply, includes #165-8001, #170-3935, and #164-5052
1658036/165-8036:小型垂直电泳槽系统Mini-PROTEAN Tetra Cell for Mini Precast Gels, Mini Trans-Blot Module, and PowerPac HC Power Supply, includes #165-8004, #170-3935, and #164-5052
Bio-Rad伯乐ReadyStrip IPG胶条1632014 1632016,Pkg of 12, 11 cm, pH 3–10, immobilized pH gradient (IPG) strip for first-dimension separations on the PROTEAN® i12™ IEF and PROTEAN IEF systems.
Durapore® Cartridge Filter with prefilter 20 in. 0.45 µm Code 7
Product Information
Device Configuration
Cartridge
Maximum Differential Pressure, bar (psid)
Forward: 5.5 bar (80 psid) @ 25 °C; 1.7 bar (25 psid) @ 80 °C; 0.35 bar (5 psid) @ 135 °C. Reverse: 3.5 bar (50 psid) @ 25 °C
Cartridge Code
Code 7 (2-226) O-rings w/locking-tabs
Good Manufacturing Practices
These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.
Prefilter Material
Mixed Cellulose Esters (MCE)
Quality Level
MQ400
Biological Information
Bacterial Endotoxins
Aqueous extraction contains ≤0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test
Media
Durapore® w/Prefilter
Sterility
Other
Sterilization
10 SIP cycles of 30 min or 10 autoclave cycles of 60 min @ 121 °C
Wettability
Hydrophilic
Physicochemical Information
Pore Size
0.45 µm
Air Diffusion at 23 °C
≤30 mL/min @ 1.5 bar (22 psig) in water
Bubble Point at 23 °C
≥1930 mbar (28 psig) air with water
Gravimetric Extractables
The extractables level was equal to or less than 45 mg per 10-inch cartridge after 24 hours in water at controlled room temperature.
Indirect Food Additive
All component materials meet the FDA Indirect Food Additive requirements cited in 21 CFR 177-182. All component materials meet the requirements of the EU framework regulation [1935/2004/EC] regarding materials and articles intended to contact food.
Non-Fiber Releasing
This product was manufactured with a Durapore® membrane which meets the criteria for a “non-fiber releasing” filter as defined in 21 CFR 210.3 (b) (6).
USP Bacterial Endotoxins
A sample aqueous extraction contains less than 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test.
Dimensions
Cartridge Nominal Length
20 in. (50 cm)
Diameter
6.9 cm (2.7 in.)
Filtration Area
1.38 m²
Device Size
20 in.
Materials Information
Chemistry
Polyvinylidene Fluoride (PVDF)
Device Material
Polypropylene
Seal Material
Silicone (SI)
Support Material
Polypropylene
Packaging Information
Material Size
3
Material Package
Double Easy-Open bag
Specifications
Oxidizable Substances
Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥2 L
规格
OptiScale® and Millipak® Capsules
OptiScale® 25 Capsules
OptiScale® 47 Capsules
Millipak® 100
Millipak® 200
Nominal Dimensions
Maximum length:
39 mm (1.52 in.) with female Luer-Lok inlet/male Luer-Lok outlet
82 mm (3.24 in.) with flange inlet/hose barb outlet 74 mm (2.91 in.) with flange inlet/flange outlet 94 mm (3.70 in.) with hose barb inlet/hose barb outlet
13 cm (5.1 in.)
15.5 cm (6.1 in.)
Diameter:
31 mm (1.21 in)
69 mm (2.75 in.)
7.6 cm (3.0 in.)
Weight:
0.19 oz (5.5 g)
2.3 oz (67 g)
—
—
Filtration Area
3.5 cm²
17.7 cm²
500 cm² (0.54 ft²)
1000 cm² (1.08 ft²)
Materials of Construction
Filter membrane:
Hydrophilic polyvinylidene fluoride (PVDF)
Structural components:
Polypropylene
Polycarbonate
Supports:
Polypropylene
Polycarbonate
Vent caps:
Polypropylene
Polyvinylidene fluoride (PVDF)
Internal seal rings:
Fluoroelastomers
—
Housing Vent
Capped Vent with female Luer connections on inlet side of device.
Adjustable vent with male luer and female Luer-Lok connections on inlet side of device.
Maximum Inlet Pressure
4.1 bar (60 psig) at 25 °C
5.5 bar (80 psig) at 25 °C
5.2 bar (75 psig) at 25 °C
Maximum Differential Pressure
Forward:
4.1 bar (60 psig) at 25 °C
5.5 bar (80 psig) at 25 °C
4.1 bar (60 psid) at 25 °C 1.7 bar (25 psid) at 80 °C 345 mbar (5 psid) at 123 °C
Reverse:
0 bar (0 psig)
0.7 bar (10 psig) at 25 °C
690 mbar (10 psid) at 25 °C
Bubble Point at 23 °C
—
—
≥ 1790 mbar (26 psig) air with water
Gravimetric Extractables
—
—
After autoclaving and a 24-hour soak in ASTM Type 1 reagent grade water at controlled room temperature:
≤ 2.5 mg
≤ 5.0 mg
Bacterial Endotoxin
Aqueous extraction contains
—
Aqueous extraction contains
Oxidizable Substances
—
Meets the requirements of the USP Oxidizable Substance Test after a water flush of:
≤ 100 mL
200 mL
200 mL
TOC/Conductivity
This product exhibited less than 500 ppb TOC per USP<643>and less than 1.3 µS per USP<645>after autoclave and a WFI water flush of 15 mL.
—
Sterilization
May be autoclaved for 1 cycle of 60 minutes at 123 °C
May be autoclaved for 3 cycles of 60 minutes at 126 °C
May be autoclaved for 3 cycles of 90 minutes at 123 °C. Capable of 45 kilogray (4.5 Megarad) gamma exposure (cannot be steam sterilized in-line).
Good Manufacturing Practices
These products are manufactured in a Millipore facility which adheres to FDA Device Good Manufacturing Practices.
Non-Fiber Releasing
Durapore membrane meets the criteria for a “non-fiber releasing” filter as defined in 21 CFR 210.3 (b) (6).
Component Material Toxicity
Component materials meet the requirements of USP<88>Reactivity Test for Class VI Plastics. This product is non-toxic per the current USP<88>Safety Test.
Indirect Food Additive
The Durapore membrane used in these products meets the FDA Indirect Food Additive requirements cited in 21 CFR 177.2910. All other components meet the FDA Indirect Food Additive requirements cited in 21 CFR 177 – 182.
Opticap® XL Capsules and Cartridge Filters
Opticap® XL 2
Opticap® XL 4
Opticap® XL 5
Opticap® XL 10
Cartridge (per 10-inch element)
Nominal Dimensions
Maximum length:
14.2 cm (5.6 in.)
19.6 cm (7.7 in.)
21.6 cm (8.5 in.)
33.5 cm (13.2 in.)
—
Diameter:
8.4 cm (3.3 in.)
10.7 cm (4.2 in.)
6.9 cm (2.7 in.)
Filtration Area
0.09 m² (0.93 ft²)
0.19 m² (2.09 ft²)
0.35 m² (3.7 ft²)
0.69 m² (7.4 ft²)
Materials of Construction
Filter membrane:
Hydrophilic PVDF
Prefilter media:
Mixed esters of cellulose
Film edge:
—
Polypropylene
Structural components:
Polypropylene
Supports:
Polypropylene
Vent O-rings:
Silicone
—
O-rings:
—
Silicone
Vent/Drain
¼ in. hose barb with double O-ring seal
—
Maximum Inlet Pressure
5.5 bar (80 psi) at 23 °C 2.8 bar (40 psi) at 60 °C 1.0 bar (15 psi) at 80 °C
Maximum Differential Pressure
Forward:
5.5 bar (80 psid) at 25 °C (with prefilter) 1.0 bar (15 psid) at 80 °C (with prefilter) 3.4 bar (50 psid) at 25 °C (without prefilter)
5.5 bar (80 psid) at 25 °C 1.8 bar (25 psid) at 80 °C 345 mbar (5 psid) at 135 °C
Reverse:
3.4 bar (50 psid) at 25 °C, intermittent
3.5 bar (50 psid) at 25 °C, intermittent
Bubble Point at 23 °C
≥ 1930 mbar (28 psig) air with water
Air Diffusion
Through a water wet membrane at ambient temperature at 1.5 bar (22 psi):
Through a water wet membrane at 23 °C at 1.5 bar (22 psi):
—
≤ 4.5 cc/min
≤ 7.5 cc/min
≤ 15 cc/min
Gravimetric Extractables
After autoclaving and a 24-hour soak in ASTM Type 1 reagent grade water at controlled room temperature:
With prefilter:
—
—
—
≤ 50 mg
≤ 45 mg
Without prefilter:
≤ 10 mg
≤ 15 mg
≤ 25 mg
≤ 20 mg
Bacterial Endotoxin
Aqueous extraction contains < 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) Test.
Oxidizable Substances
Meets the requirements of the USP Oxidizable Substance Test after a water flush of:
500 mL
1000 mL
Sterilization (with Prefilter)
Autoclaved:
3 cycles of 60 minutes at 121 °C.
10 cycles of 60 minutes at 121 °C
Steam Sterilization:
Cannot be steam sterilized in-line.
10 cycles of 30 minutes at 121 °C
Hot Water Sanitization:
—
30 cycles of 30 minutes at 80 °C
Sterilization (without Prefilter)
Autoclaved:
3 cycles of 60 minutes at 126 °C
30 cycles of 60 minutes at 126 °C
Steam Sterilization:
Cannot be steam sterilized in-line.
30 cycles of 30 minutes at 135 °C
Hot Water Sanitization:
—
30 cycles of 30 minutes at 80 °C
Total Organic Carbon (TOC)/Conductivity
Autoclaved filter effluent meets the WFI requirement of USP<643>, for Total Organic Carbon and USP<645>for Water Conductivity at 25 ºC after a WFI flush of 11.5 L
Good Manufacturing Practices
These products are manufactured in a Millipore facility which adheres to FDA Good Manufacturing Practices.
Non-Fiber Releasing
Durapore membrane meets the criteria for a “non-fiber releasing” filter as defined in 21 CFR 210.3 (b) (6).
Component Material Toxicity
Component materials were tested and meet the criteria of the USP<88>Reactivity Test for Class VI Plastics. Sterilizing-grade Durapore Filters are non-toxic per the current USP<88>Safety Test.
Indirect Food Additive
Durapore membrane meets the FDA Indirect Food Additive requirements cited in 21 CFR 177.2910. All other component materials also meet the FDA Indirect Food Additive requirements cited in 21 CFR 177 – 182.
European Pressure Equipment Directive
Millipore Corporation certifies that this product complies with the European Pressure Equipment Directive, 97/23/EC of 29 May 1997. This product has been classified under Article 3 § 3 of the Pressure Vessel Directive. It has been designed and manufactured in accordance with sound engineering practice to ensure safe use. In compliance with Article 3 § 3 of this Pressure Equipment Directive, this product does not bear the CE mark.