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108-20-3
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关键词:'108-20-3'
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Steritest™ Syringe Support User Guide - CHINESE
与某些末端为鲁尔锁
定公头的注射器也兼容。在使用注射器支架之前，检查这些注射器的尺寸和任何
其他设计是否与其Steritest™装置的样品相配。欲悉详情，请联络您当地的销售代
表。
20
3. 轻轻拧松支臂的固定螺钉，上下左右调节支臂的位置，使支臂在接近注射器筒远端
（与针头尖相反的位置）的地方支撑注射器。把支臂调到正确位置后，拧紧支臂固
定螺钉。
说明：
Mid-Infrared-based quantitation of highly modified proteins, labeled peptides and peptidomimetics
62164.2 111.5 27 20 59310 1.01 604 103.6
STDEV 603 66776 3.4 31 24 65792 0.51 653 3.4
Max. 34350 3816037 138.3 942 1111 3991820 5.26 36402 166.9
Min. 4 500.6 82.6 0 0 0 0 3 65
CV 108% 107% 3% 118% 121%
Quality Control Range Sheet- HNDG1-108 and HNDG1-208
Lot # Expected Range Units
APOA-1 Control I HNDG1-108 13 - 28 ng/mL
Control II HNDG1-208 66 - 137 ng/mL
APOC-3 Control I HNDG1-108 0.22 -
MILLIPLEX®MAP Human Myokine Panel is an optimized quantitative immunoassay that simultaneously measures 15 novel muscle-secreted factors
19 16 20 18 101 52 35 112 6886 53 31 34 35 153 29
std
7
23 14 20 21 108 51 30 113 12255 51 31 36 34 156 28
20 15 20 18 104
Data Sheet - 83913
solution per
108 cells. This solution can be stored one month at room temperature.
2. Add 10ml of solution D per 108 cells. Mix thoroughly and allow to sit 1 min at room
temperature.
Data Sheet - C8406
assay and control tubes for
approximately 20 minutes in a 37 °C water bath.
6. Prepare a
Insert Sheet Chromolith Prep Si & RP-18e
us to trace the manufacturing
history of your column.
11-108-5_PB_Chromolith prep SI:S000002122_Chromolith prep SI 16.11.11 09:56 Seite 3
1.3.1 Installation of the Column
Connect your
Charged filter endotoxin removal performance comparison
charged membrane
108
(breakthrough point
not reached)
>8.2 x 108 >6.04 x 108
Figure 4.
Observed endotoxin
concentrations
Figure 3.
5% mannitol
solutions spiked with
of 108 EU/mL (trial 1
QCM™ Endothelial Cell Migration Assay
CD
0
1.0×107
2.0×107
3.0×107
4.0×107
5.0×107
6.0×107
7.0×107
8.0×107
9.0×107
1.0×108
1.1×108
1.2×108
1.3×108
1.4×108
BSA
FBS
BSA+Lat
FBS+Lat
BSA+CD
FBS+CD
Fl
uo
re
sc
en
ce
in
te
ns
The Effective Use of Protein Kinase Inhibitors
102 111 101 93 97 108 101 98 92 89 95 91 100
JNK/SAPK1c
SAPK2a/p38 99 94 93 111 95 75 100 85 2 0 86 98 138 93 108 102 84 88 104
SAPK2b/p38β2 97 107
Product Information Sheet - PEROX1
prepare a minimum
of 2 × 108 cells and 10 mL of buffer.
1× OptiPrep™ Dilution Buffer
1. Dilute an aliquot of the OptiPrep™ Dilution Buffer
20× (Component O4889) 20-fold with water.
The Effective Use of Protein Kinase Inhibitors
102 111 101 93 97 108 101 98 92 89 95 91 100
JNK/SAPK1c
SAPK2a/p38 99 94 93 111 95 75 100 85 2 0 86 98 138 93 108 102 84 88 104
SAPK2b/p38β2 97 107
ERalpha Ms-Cy5 SmartFlare™ RNA Detection Probe
R
ev
A
/2
01
3/
02
/1
2/
S
F-
10
8D
S
C
A
/A
K
0
10
20
30
40
Data Sheet - P0061
nmole/min/mg = ∆cpm × (25/20)
SR × E × T
SR = specific radioactivity of the ATP (cpm/nmole ATP)
∆cpm = cpm of the sample – cpm of the blank (step 3)
25 = total reaction volume
20 = spot volume
T
Technical Brief: Viresolve®Prefilter: Extractables Characterization
Post Viresolve®
Prefilter (ppb)
Post-10x UF 5x DF
(ppb)
USP WFI MCL
(ppb)
Aluminum 108 20 194 20 50
Arsenic 2.6 NA 11 5.0 50
Iron 22 32 264 44 300
Lead 2.2 NA <
Data Sheet - C8567 - Lot 083H9480
deionized water in the amount given on the label.
2. Add 20 µl of a solution containing 0.3 M CaCl2
and 1 M MgCl2 to each ml of C1q deficient serum.
3. Prepare nine precooled assay tubes labeled "A"
through
Data Sheet - C8567 - Lot 049H9276
serum with 1 ml ice
cold deionized water.
2. Add 20 µl of a solution containing 0.3 M CaCl2 and
1 M MgCl2 to each ml of C1q deficient serum.
3. Dilute an aliquot of the C1q deficient serum with
gelatin
N-TER/siRNA nanoparticle mediated knockdown of gene expression
10 or 20 nM
Reagent
(µL)
96-well plate 48-well plate 24-well plate 12-well plate 6-well plate
10 nM / 20 nM 10 nM / 20 nM 10 nM / 20 nM 10 nM / 20 nM 10 nM
Validation and Qualification for Durapore® Sterilizing-Grade (0.22 µm) Membrane VMF4
61 15.0 >8.22 114
3 10.0 4.22 116 62 16.2 >8.22 94
1 10.2 4.29 117 63 16.0 8.22 96
21 10.2 4.30 118 7 13.6 >8.29 106
20 10.3 4.35 113 10 14.1 >8.29 99
SIRTainty™ Class III HDAC Assay
ity
SIRT (Units)
SIRT1, Km = 1 unit
SIRT2, Km = 0.14 unit
SIRT3, Km = 0.19 unit
1.0 x 108
10 15 20 25
0.0
2.0 x 107
H4
4.0 x 107
6.0 x 107
Separation of some chlorophenols
Acetonictrile/water 80/20 (v/v)
Migration Distance 7 cm
Chamber Normal chamber without chamber saturation
Compounds 1. Pentachlorophenol
2. 2,4,6-Trichlorophenol
3. 2,4-Dichlorophenol
Data Sheet - C8406 - Lot 010K4044
all assay and control tubes for
approximately 20 minutes in a 37EC water bath.
6. Prepare a suspension
Product Information - L6787
Allopurinol
B7283 Benserazide hydrochloride
B8132 S(-)-p-Bromotetramisole oxalate
B8279 Ro 20-1724
C-108 2-Cyclooctyl-2-hydroxyethylamine
hydrochloride
C-126 S-(-)-Carbidopa
C2932 Chelerythrine
Data Sheet - L6787
Allopurinol
B7283 Benserazide hydrochloride
B8132 S(-)-p-Bromotetramisole oxalate
B8279 Ro 20-1724
C-108 2-Cyclooctyl-2-hydroxyethylamine
hydrochloride
C-126 S-(-)-Carbidopa
C2932 Chelerythrine
Quality Control Ranges: Human Circulating Cancer Biomarker Magnetic Bead Panel 3
Biomarker
MILLIPLEX® MAP Magnetic Bead Panel 3
Kit Catalog # HCCBP3MAG-58K
Control Catalog # HCC3-6058-3
Lot# HCC3-108 and HCC3-208
HCC3-6058-3: HCC3-108.208 (07 August 2020)
EMD Millipore
Magna ChIP2 TM Chromatin Immunoprecipitation DNA Microarray Universal Kit
limiting, 1 x 108 cells is a
useful guideline quantity.
• Stimulate or treat, if necessary, adherent mammalian cells at ~80-90% confluence in a 150
mm culture dish containing 20 mL of growth
Competent Cell Brochure
cloning
Singles™ > 1.5 × 108 50 µl Routine cloning
Veggie™ > 1.5 × 108 50 µl Applications requiring
nonanimal-derived materials
Routine cloning
HT96™ > 1.0 × 108 96 x 20 µl High-throughput cloning
Insert Sheet Particulate analytical HPLC columns
using wrenches.
Figure 1
Figure 2
Figure 4 Figure 5 Figure 6
11-108-2_PB HPLC columns:PB 03.11.11 15:18 Seite 3
Made in Germany
Merck KGaA, 64271
Product Information Sheet - RPROTKRO
;23:77.
2 Wieger U & Hilz H. Biochem. Biophys. Res. Commun. (1971);44:513.
3 Hilz, H. et al. Eur. J. Biochem. (1975);56:103–108.
4 Sambrook J et al. Molecular Cloning: A Laboratory Manual, 2nd edition
Complement C2 Deficient Serum (C0913)
purified C2*
(µl)
EA7S
(1.5 × 108 cells/ml)
(µl)
GVB2+
(µl)
Distilled
water
(µl)
A** v – 200 300–v –
B v 5 200 295–v –
C v 10 200 290–v –
D v 20 200
1/32