Professional Documents
Culture Documents
・OneSTEP Ladders
・Ladders for 10minute separation
・Wide Range Ladders
・Markers & OneSTEP Markers Size St
・RNA Si Standard
d Markers
・DGGE Markers ・RNA Step Ladder
・PCR Marker Makers ・Loading Buffers
Molecular-Weight
Markers
・Easy SeparatorTM
・Negative Gel Stain MS Kit
・SuperSepTM Ace
・Prestain markers ・SuperSepTM DNA
・Western marker
・Biotinylated marker
・Markers for CBB dyeing
DNA Ladder
DNA Ladder
DNA Step Ladder (1~6) Ready With dye and glycerol already
to added, it is ready to be applied to
use the agarose gel.
for low-molecular-range analysis.
3.5% Agarose
50 100
2% Agarose
2% Agarose
1% Agarose
10 50 80
25 25 80 50
1 2 3 4
OneSTEP Ladder (7~12)
for simultaneous measurement of DNA size and amount.
DNA Step Ladder 100 bp DNA Step Ladder OneSTEP Ladder 50 OneSTEP Ladder 100
(10-300 bp) (0.1-1.5 kbp) (0.05-2 kbp) (0.1-2 kbp)
(bp) (bp) (bp)(ng/5µL) (bp)(ng/5µL)
Ready −20℃ Ready 2,000 100 Ready
to 300 1,500 to to 2,000 100
use 1,000 use 1,500 75 use 1,800 90
200 1,000 50 1,600 80
900 900 45
−20℃ 150 800 40 1,400 70
6x 800
Loading 700 35 1,200 60
100 Dye 717 1,000 100
75 600 30
600 500 75 900 45
6x 50 400 22.5 800 40
Loading
Dye 35 500 450 20 700 35
25 400 350 17.5 600 30
20 300 15 500 50
5% Agarose 21
3% Agarose 21
3% Agarose 21
250 37.5
15 286 200 10 400 20
2% Agarose
100 50 100
5 Loading:
5-10µL/lane
6 Loading:
5µL/lane
7 Concentration:
0.69µg/5µL
8 Concentration:
0.755µg/5µL
OneSTEP Ladder 500 OneSTEP Ladder 1 kb OneSTEP Ladder Gene Ladder 100
(0.5-5 kbp) (1-10 kbp) Supercoiled Plasmid (0.1-2 kbp)
2% Agarose S
1% Agarose S
1% Agarose S
9 each fragment:
50ng/5µL 10 each fragment:
50ng/5µL 11 each fragment:
30ng/5µL 12 Concentration:
0.64µg/5µL
2
Ladder for 10minute separation (13~18) −20℃
: Store at ー20℃
NO DISPLAY: Store at 2∼10℃
DNA Step Ladder DNA Step Ladder DNA Step Ladder DNA Step Ladder Gene Ladder Fast 1
(10-200 bp) (50-1,500 bp) (100-5,000 bp) (500-10,000bp) (4 bands:0.1-2 kbp)
1% Agarose S
Ready Ready (bp) Ready (bp) Ready Ready
to to to to to
use use use use use
10,000
−20℃ −20℃ −20℃ 5,000 −20℃ 4,000 2,000 25
200 2,000 2,000 1,000 25
100 1,500 500 25
6x 6x 6x 6x 1,000 100 25
Loading 50 Loading
850 Loading 850 Loading
Dye Dye Dye Dye
20 500 17 Concentration:
4% Agarose 21
400 400
10 0.1µg/5µL
2% Agarose
2% Agarose
2% Agarose
200
100 Gene Ladder Fast 2
50 (6 bands:0.1-10 kbp)
1% Agarose S
Ready (bp)
(ng/5µL)
to
use
Loading: Loading: Loading: Loading: 10,000 25
20µL/lane 20µL/lane 20µL/lane 20µL/lane 4,000 25
2,000 25
1,000 25
500 25
100 25
13 14 15 16 18
Concentration:
0.15µg/5µL
3
DNA Ladder
DNA Ladder
der (19~22)
Wide Range Ladder
for wide-range and simultaneous analysis
l i off b
both
th DNA size
i and
d amount.
t
DNA Step Ladder Mix Smart Ladder Gene Ladder Wide 1 Gene Ladder Wide 2
(0.08-10 kbp) (0.2-10 kbp) (0.1-20 kbp) (0.1-20 kbp)
800 80
800 160 1,000 100 900 45
600 60 800 40
700 140
600 120 400 40 700 35 700 35
200 20 500 75 600 30
1% Agarose
1% Agarose
500 200 500 75
400 80 400 40
1% Agarose
300 30 400 40
300 60 200 20 200 20
200 40 100 100 100 100
19 100
80
20
16
20 21 22
Ready
Marker −20℃ & the OneSTEP Marker to
use (23~33)
DNA molec
molecular-weight
lar eight markers that set si
size
e standards for linear do
double-strand
ble strand DNA
DNA. EEach One-Step Marker
comes with pre-added dye and glycerol, so they can be applied directly to the agarose gel.
2.32 271
1% Agarose S
1% Agarose S
1% Agarose S
1.58
2.02 234
1.38
194
0.95
118
23 24 0.83 25 26 72
0.3% Agarose H
291 1.88
3% Agarose 21
210 8.03
1% Agaose S
162 1.49
5.59
0.93 5.51
27 79 28 29 30
4
Marker 9 Marker 10 Marker 11
(φX174/HinfⅠ) (pBR322/MspⅠ) (pUC19/MspⅠ)
3% Agarose 21
160
3% Agarose 21
3% Agarose 21
140 110
147
118 147
100 123
82 110
66 90
31 66
48 32 76
67 33
Number Product name Code No. Package Size Note
19 DNA Step Ladder Mix(0.08-10 kbp) 292-68401 1 mL
313-03943 25 μL
20 Smart Ladder (0.2-10 kbp)
317-03941 500 μL
21 Gene Ladder Wide 1(0.1-20 kbp) 313-06961 500 μL × 2
22 Gene Ladder Wide 2(0.1-20 kbp) 310-06971 500 μL × 2
310-05251 1500 μL
OneSTEP Marker 1(lambda/ d Ⅲ digest)
314-05254 1500 μL × 5
23
316-00454 120 μg
Marker 1(lambda/ d Ⅲ digest)
312-00456 120 μg × 5
OneSTEP Marker 2 317-05261 1500 μL
(lambda/ dⅢ+ R I double digest) 311-05264 1500 μL × 5
24
Marker 2 319-00564 80 μg
(lambda/ dⅢ+ R I double digest) 315-00566 80 μg × 5
OneSTEP Marker 3 314-05271 1500 μL
(lambda/ d Ⅲ + lambda/ R I digest mixture) 310-05273 1500 μL × 5
25
Marker 3 316-00574 80 μg
(lambda/ d Ⅲ + lambda/ R I digest mixture) 312-00576 80 μg × 5
318-05791 375 μL
OneSTEP Marker 4(phiX174/ Ⅲ digest)
314-05793 375 μL × 5
26
315-00664 15 μg
Marker 4(phiX174/ Ⅲ digest)
311-00666 15 μg × 5
311-05801 375 μL
OneSTEP Marker 5(phiX174/ c Ⅱ digest)
317-05803 375 μL × 5
27
312-00674 15 μg
Marker 5(phiX174/ c Ⅱ digest)
318-00676 15 μg × 5
311-05281 1500 μL
OneSTEP Marker 6(lambda/ Ⅰdigest)
317-05283 1500 μL × 5
28
313-00964 80 μg
Marker 6(lambda/ Ⅰdigest)
319-00966 80 μg × 5
315-03981 10 μg
29 Marker 7 GT
311-03983 10 μg × 5
312-03991 10 μg
30 Marker 8 GT
318-03993 10 μg × 5
318-05811 375 μL
OneSTEP Marker 9(phiX174/ fⅠdigest)
314-05813 375 μL × 5
31
314-01491 15 μg
Marker 9(phiX174/ fⅠdigest)
310-01493 15 μg × 5
315-05821 375 μL
OneSTEP Marker 10(pBR322/ Ⅰdigest)
311-05823 375 μL × 5
32
317-01501 15 μg
Marker 10(pBR322/ Ⅰdigest)
313-01503 15 μg × 5
312-05831 375 μL
OneSTEP Marker 11(pUC19/ Ⅰdigest)
318-05833 375 μL × 5
33
319-03261 15 μg
Marker 11(pUC19/ Ⅰdigest)
315-03263 15 μg × 5
5
DNA Ladder
DNA Ladder
DGGE MarkerⅠ DGGE Marker Ⅱ DGGE Marker Ⅲ DGGE Marker Ⅳ DGGE Marker Ⅴ
(5 fragments) (10 fragments) (10 fragments) (8 fragments) (9 fragments)
8% Acrylamide
7% Acrylamide
6% Acrylamide
6% Acrylamide
5 9 9
8
10 10
RNA Ladder
RNA Size Standard Marker (1~4)
RNA molecular-weight markers prepared by in vitro transcription.
RNA Size Standard RNA Size Standard RNA Size Standard RNA Ladder
Marker Ⅱ Marker Ⅲ (0.1-1 kb) Marker Ⅳ (0.28-6.58 kb) (0.125-6 kb)
1% formaldehyde Agarose
5 400 3,638 3,000
2,000
4 300 2,604
1,500
1,908 1,000
1% formaldehyde Agarose
1% formaldehyde Agarose
3
500
5% polyacrylamide-urea
RNA Step Ladder (0.1–1 kb) (5) Loading Buffer (Store at room temp.)
an RNA molecular-weight
l l i ht marker
k can b be di
directly
tl applied
li d A sample can be easily applied during DNA gel
to native gel, denatured gel, or polyacrylamide gel. electrophoresis to effectively predict the migration
point.
a b c d e f a b c d e f
RNA Step Ladder (0.1-1 kb)
Xylene Cyanol FF
−80℃ (base) (base)
Bromophenol Blue
2X 1,000 1,000
Loading 800 800
Dye Orange G
600 600
2% Formaldehyde Agarose
400 400
300 a Marker 4 6 × Loading Buffer Triple Dye
300 b (φX173/Hae Ⅲ) 6 × Loading Buffer Orange G
2% Native Agarose
5 1 % agarose S
2 % agarose S
100 bp (approx.) 900 bp (approx.) 5,000 bp (approx.)
30 bp (approx.) 300 bp (approx.) 1,500 bp (approx.)
3 % agarose 21 10 bp (approx.) 100 bp (approx.) 500 bp (approx.)
Prestained Marker (1, 2) : With dye combined in its recombinant protein content.
Western Marker (3) : Contains protein G with the ability to combine with the Fc region
of immunoglobulin. Reacts with both primary and secondary
antibodies in a western blot.
Biotinylated Marker (4) : Contains biotinylated protein. Capable of both chromogenetic and
photogenetic detection by reacting with avidin HRP or avidin AP.
200 180
116
116 97
79
79 79
42
42
42 42
30 30
30 30
20 20
20 17
14
17 14
6.5 6.5
3.5
−20℃
: Store at ー20℃
NO DISPLAY: Store at 2∼10℃
8
Electrophoresis-related Products
Electrophoresis-related Products
Easy SeparatorTM (Wako Catalog No.058-07681 (1 set ) )
Easy SeparatorTM is an electrophoresis tank specially designed for “SuperSep” products to enable easy setting
and removal of the gel plate.
Features
1 Easy to operate.
2 Requires only a small amount (about 250-350ml) of
running buffer for electrophoresis.
3 Allows the gel plate to be removed without removing the
running buffer after electrophoresis has been completed.
①Insert a gel. ②Turn the knobs ③Setting is ①Remove the cover ②Turn the knobs ③Remove the gel
toward you. completed. after electrophoresis away from you. without removing
has been completed. the running buffer.
Protein bands separated by SDS/polyacrylamide gel electrophoresis (SDS-PAGE) can be visualized as stable,
clear and transparent bands against the background of milky white gel stained by negative gel stain containing
our improved imidazol derivative reagent in as little as 10 minutes. The staining technique is useful to obtain the
clear and sensitive resolution pattern of the gel before immunoblotting as well as to excise and purify the band
of interest from the gel without significant deterioration of amino acid residues for the subsequent studies of
protein such as sequencing and mass analysis of peptide.
Procedure Featureas
SDS-PAGE gel 1 Detectable limit of protein: 1 ng
Staining Sol. A 2 Sensitive and Simple procedure with 2-step staining in
Shake 5 10 min. 5~10 minutes
Wash 5 10 sec. x 3
3 Optimized the staining intensity by either de-staining the
Staining Sol. B excess stain or re-staining following de-stain of the gel.
Shake 10 60 sec.
Wash 1 min. x 3 4 Applicable to proteome analysis by mass spectrometry
and sequencing
Check staining intensity
of the gel against a sheet
Mass Spectrometry of black paper MALDI-TOF/MS analysis
rat muscle glycogen phosphorylase (EC2.4.1.1)
SDS-PAGE analysis
relative abundance
1 2 3
a Figure 1.
b SDS-PAGE analysis of proteins using
Figure 2.
Negative Gel Stain MS Kit
c MALDI-TOF/MS of
a : rat phosphorylase (97k); 1000 1100 1200 1300 1400 1500 1600 1700 1800 1900 2000 rat phosphorylase
b : bovine serum albumin (68k); m/z
d c : hen egg white ovalbumin (45k); The band was excised and treated with trypsin. Following the in-gel digestion and
d : bovine carbonic anhydrase (31k). preparation, the sample was analyzed on MALDI-TOF mass spectrometer. (These data
Lane 1: 50 ng; Lane 2: 100 ng; Lane 3: 150 ng were provided by Dr. Y. Wada at Osaka Medical Center, Japan.)
9
Electrophoresis-related Products
Electrophoresis-related Products
SuperSepTM Ace
SuperSep™ Ace is a polyacryla
polyacrylamide
amide gel of the highest quality
quality, 13 well 17 well
designed to resolve the problems of existing products (SuperSep™ and
SuperSep™ HG). Tris-glycine buffer is used in the gel buffer, similar to
existing products, but because its pH is neutralized, the gel’s chemical
storage stability is improved. Physical storage stability is also improved
by using vacuum packaging. And because it does not contain SDS, it
can be used in SDS-PAGE and Native-PAGE by changing the running
t
buffer. enien
Conv er for
stick el
g n!
Features n t if icatio
ide
1 Good separation and uniform bands
2 Can be used with a multi-channel pipette.
3 Reasonably priced and capable of long-term storage (for 6 months)
4 Box sticker allows easy identification of type of gel.
5 Comes in 13-well and 17-well types.
oved
Impr ation
r
Product specifications sepa center!
th e
Plate size 100 × 100 × 3(mm) near SuperSepTM SuperSepTM
Ace
Gel size 90 × 85 × 1(mm) (kDa)
Number of wells 13 wells 17 wells 200
30 μL 25 μL 150
Well volume
100
Total amount of protein* (/well) 3.3 ∼ 6.5 μg 1.3 ∼ 3.9 μg 75
*Indicates total amount of protein that can be clearly separated.
50
rm
Unifo d!
37
① SuperSepTM: 10%
ban 0 1.5 3 4.5 6 7.5 9 10.5 12 (hours)
25
TM
②SuperSep Ace: 10% 20
(Store at 2∼10℃)
10
SuperSepTM DNA (15%, 17 wells) (Wako Catalog No.190-15481 (10 ea.) ) (Store at 2∼10℃)
Polyacrylamide gel is used in the separation of low-molecular-weight DNA because it has a finer gel mesh
structure than agarose. However, the DNA size will vary widely depending on the acrylamide concentration and
the degree of cross-linkage of the gel. In SuperSepTM DNA, the acrylamide concentration and the degree of
cross-linkage of the gel have been optimized for the separation of low-molecular-weight DNA. This product is
therefore effective for the separation of samples with a DNA size from 20-200 bp.
100
90
80
200
70 200
60 150 150
100
50
90 100
40 100
80
30 70 75 75
20 60 50
50 50
40 25
30
25
20
Example of electrophoresis
20-200 bp DNA was clearly separated by using SuperSepTM DNA and Tris-glycine buffer. PCR products under 200
bp can be used for separation from gel, especially when cloning small RNA. 30-200 bp DNA was clearly
separated with TBE buffer.
200
150 200
100 150
100
50
50
30
25 30
20 20 25
Staining Reagent
Product name Wako Cat. No. Package Size
EtBr Solution 315-90051 10 mL
11
Selection Guide
【How to read the chart】 【Display codes】
● 1 , p1 NO DISPLAY Store at 2∼10℃ −80℃ Store at or below ー80℃
Number Reference page −20℃ Store at or below ー20℃ −70℃ Store at or below ー70℃
DNA Ladders
10 bp 100 bp 1 kbp 10 kbp 100 kbp 200 kbp
●
1 , p2
●
2 , p2
●
3 , p2
●
4 , p2
●
5 , p2
●
6 , p2
●7 , p2
●8 , p2
●
9 , p2
●
10 , p2
●
11 , p2
●
12 , p2
●
13 , p3
●
14 , p3
●
15 , p3
●
16 , p3
●
17 , p3
●
18 , p3
●
19 , p4
●
20 , p4
●
21 , p4
●
22 , p4
●
23 , p4
●
24 , p4
●
25 , p4
●26 , p4
●
27 , p4
●
28 , p4
●
29 , p4
●30 , p4
●
31 , p5
●
32 , p5
●
33 , p5
●
39 , p6
●
40 , p6
●
41 , p6
●
42 , p6
RNA Ladders
10 b 100 b 1000 b 10000 b
●
1 , p7
●
2 , p7
●
3 , p7
●
4 , p7
●
5 , p7
●
1 , p8
●
2 , p8
●
3 , p8
●
4 , p8
●
5 , p8
●
6 , p8
●7 , p8
●
8 , p8
・This brochure may contain products that cannot be exported to your country due to regulations.
・Listed products are intended for laboratory research use only, and not to be used for drug, food or human use.
co.jp
08X05開01
09Y3IBF