CN
tweezers
应用筛选条件
关键词:'tweezers'
显示 1-30 共 87 条结果 关于 "tweezers" 范围 技术文档
AL-266 Self-Assembly Tech Spotlight
clean tweezers and rinse with solvent for
10–15 seconds using a clean solvent bottle.
Note: For thiols with hydrogen-bonding, polar
or bulky head groups, hold sample with clean
tweezers and rinse
Bulletin - 687804
conditions, but a full vacuum is
necessary for optimal release.
Pick-up Tools - The largest tweezers tool compatible
with the array size should be used in order to deliver
the maximum twist or rotation
Bulletin - 687812
conditions, but a full vacuum is
necessary for optimal release.
Pick-up Tools - The largest tweezers tool compatible
with the array size should be used in order to deliver
the maximum twist or rotation
Harvesting Multi-cellular Microtissues from 3D Petri Dishes
microtissues have been released.
5. Remove the empty 3D Petri Dish® with a sterile spatula or sterile tweezers.
6. The harvested multi-cellular microtissues remaining in the cell culture medium can be
Product Information Sheet - GRFETS20
precautions:
• Be careful when handling the GFET chip that tweezers do not make contact with the device area.
Metallic tweezers should be avoided, as they can damage/scratch the chip edges/surface
User Guide
Coverslip
Using tweezers carefully place a coverslip
on top of the slide without disturbing the
probe-hybridization buffer mixture.
7e. Place in Hybridization Oven
Using tweezers carefully place
Product Information Sheet -MBD0059
Coverslip
Using tweezers carefully place a coverslip
on top of the slide without disturbing the
probe-hybridization buffer mixture.
7e. Place in Hybridization Oven
Using tweezers carefully place
Product Information Sheet - GRFETS10
precautions:
• Be careful when handling the graphene FET chip. Tweezers should not contact the device area directly.
Metallic tweezers should be avoided, since they can damage/scratch the chip’s surface
Product Information Sheet - RP2
thickness blotting paper and dispose.
Carefully remove the gel. Carefully remove the
membrane with tweezers and place on blotting
paper. Dispose of the QuickDraw sheets. Rinse
each tray with deionized water
Product Information Sheet - RAPID1
thickness blotting paper and dispose.
Carefully remove the gel. Carefully remove the
membrane with tweezers and place on blotting
paper. Dispose of the QuickDraw sheets. Rinse
each tray with deionized water
Product Information Sheet - RP3
thickness blotting paper and dispose.
Carefully remove the gel. Carefully remove the
membrane with tweezers and place on blotting
paper. Dispose of the QuickDraw sheets. Rinse
each tray with deionized water
Product Information Sheet - RAPID2
thickness blotting paper and dispose.
Carefully remove the gel. Carefully remove the
membrane with tweezers and place on blotting
paper. Dispose of the QuickDraw sheets. Rinse
each tray with deionized water
Product Information Sheet - RP4
thickness blotting paper and dispose.
Carefully remove the gel. Carefully remove the
membrane with tweezers and place on blotting
paper. Dispose of the QuickDraw sheets. Rinse
each tray with deionized water
Product Information Sheet - RP1
thickness blotting paper and dispose.
Carefully remove the gel. Carefully remove the
membrane with tweezers and place on blotting
paper. Dispose of the QuickDraw sheets. Rinse
each tray with deionized water
Data Sheet - 05904
sample dipstick from the blood collection area, perforated for easy removal from the
device, with tweezers (for the double-test), and place each sample into a 10 mL screw cap vial containing
1 mL 1.25 M
Userguide -XX2702550
or
soft-nosed tweezers.
2. Place the filter in a container
of deionized water to wet it
completely.
3. Remove the filter from the water using the forceps
or soft-nosed tweezers and center it on
Product Information Sheet - PROTRA
blade, taking care to include only stained gel.
Lift out the gel piece using clean flat nosed
tweezers.
2. Place the gel piece in a siliconized microtube. A
siliconized tube reduces binding of the
Technical Bulletin - PP0100
blade, taking care to include only stained gel.
Lift out the gel piece using clean flat nosed
tweezers.
2. Place the gel piece in a siliconized Eppendorf tube
or equivalent. A siliconized tube
100820 Methenamine silver plating kit acc. to Gomori for the detection of argent-affine structures in histological tissue
slides in the conventional manner and rehydrate
in a descending alcohol series.
Do not use metal tweezers and do not allow any other metal objects to
come into contact with the slides.
The stated times
Product Information Sheet - PP0200
razor blade, taking care to include only
stained gel. Remove the gel piece using clean flat
nosed tweezers.
Note: The gel piece may be cut into equal sections
of 1 to 1.5 mm size and the sections may
Product Information Sheet - EMS0006
scalpel or razor blade,
taking care to include only stained gel. Lift out the
gel piece using clean tweezers.
2. Place the gel piece in a siliconized tube or
equivalent. A siliconized tube reduces binding
Product Information Sheet - EMS0007
scalpel or razor blade,
taking care to include only stained gel. Lift out the
gel piece using clean tweezers.
2. Place the gel piece in a siliconized tube or
equivalent. A siliconized tube reduces binding
Perfusion Bioreactor Details
Bioreactor
Loading:
Parts
©
3D
BIOTEK,
LLC
Bioreactor
Chamber
Tweezers
O-‐Ring
Pusher
O-‐Rings
3D
Inserts
20
Product Information Sheet - EMS0004
scalpel or razor blade,
taking care to include only stained gel. Lift out the
gel piece using clean tweezers.
2. Place the gel piece in a siliconized tube or
equivalent. A siliconized tube reduces binding
Technical Support- 3D Perfusion Bioreactor Assembly
Bioreactor
Loading:
Parts
©
3D
BIOTEK,
LLC
Bioreactor
Chamber
Tweezers
O-‐Ring
Pusher
O-‐Rings
3D
Inserts
20
Product Information Sheet - EMS0005
scalpel or razor blade,
taking care to include only stained gel. Lift out the
gel piece using clean tweezers.
2. Place the gel piece in a siliconized tube or
equivalent. A siliconized tube reduces binding
ReBlot Plus Kit - Data Sheet
Antibody
Stripping Solution (see Preparation of Reagents for suggested quantities).
2. Using tweezers or forceps, submerge blot or blot strips in stripping solution.
Incubate with gentle mixing for
102414 Warthin-Starry silver plating kit modified for the detection of Helicobacter pylori in paraffin sections
slides in the conventional manner and rehydrate
in a descending alcohol series.
Do not use metal tweezers and do not allow any other metal objects to
come into contact with the slides.
The stated times
Product Information Sheet - A6487
razor blade, taking care to include
only stained gel. Lift the gel piece out with
clean flat-nosed tweezers.
2. Place the gel piece in a siliconized
microcentrifuge tube or equivalent.
Notes: A siliconized
Re-Blot Plus Western Blot Recycling Kit
Antibody
Stripping Solution (see Preparation of Reagents for suggested quantities).
2. Using tweezers or forceps, submerge blot or blot strips in stripping solution.
Incubate with gentle mixing for
1/3