Goat Anti-Rabbit (GAR) Conjugated Colloidal Gold for Lateral Flow (1mL of 10OD)
Product image shows functional testing of Goat Anti Rabbit 40nm colloidal gold on a lateral flow test.
Our products are produced in a state-of-the-art manufacturing facility that enable rapid turnaround times while ensuring batch to batch consistency and reliability.
Goat Anti-Rabbit (GAR) Conjugated Colloidal Gold for Lateral Flow (1mL of 10OD)
Product image shows functional testing of Goat Anti Rabbit 40nm colloidal gold on a lateral flow test.
Our products are produced in a state-of-the-art manufacturing facility that enable rapid turnaround times while ensuring batch to batch consistency and reliability.
The Primerdesign genesig Kit for Shigella species (Shigella_spp) genomes is designed for the in vitro quantification of Shigella_spp genomes. The kit is designed to have a broad detection profile. Specifically, the primers represent 100% homology with over 95% of the NCBI database reference sequences available at the time of design.
The dynamics of genetic variation means that new sequence information may become available after the initial design. Primerdesign periodically reviews the detection profiles of our kits and when required releases new versions.
The target sequence is within the virulence plasmid pCP301 (VirA) which is carried by nearly all clinical isolates of shigella. This target has previously been shown to be a good genetic marker for Shigella in other real time PCR based studies (Hiroshi Fukushima et.al 2003.) The primers and probe sequences in this kit have 100% homology with over 95% of reference sequences in the NCBI database based on a comprehensive bioinformatics analysis.
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Exceptional value for money Rapid detection of all clinically relevant subtypes Positive copy number standard curve for quantification Highly specific detection profile High priming efficiency Broad dynamic detection range (>6 logs) Sensitive to < 100 copies of target
Accurate controls to confirm findings
It’s widely used in the field of animal and plant molecular biology, which is the ideal instrument for seperating the chemical substances in the cell and purifing the microorganisms, viruses, bacteira and subcelluar etc.
TG18 High Speed/Low Speed Centrifuge Features:
1. Max. Speed 21000rpm, max. volume 4x800ml, can be used for 5ml/10ml/15ml/30ml/50ml/100ml centrifuge tubes.
2. Brushless DC motor in great torque, no powder pollution, free maintenance, quick in speed up and down.
3. Can store 10 programs, automatically calculate and synchronously display the RCF data. Digital display indicates the speed, time, temperature and RCF. The parameters can be changed in operation, no need to stop the centrifuge which is quite convenient.
4. The centrifuge body is made of high-quality steel, and with high-quality steel centrifuge chamber, safe and reliable.
5. Automatically electric lid lock, over speed/over temperature protection and imbalance protection.
6. There are many kinds of rotors for your choice, both in high speed and low speed.
TG18 High Speed/Low Speed Centrifuge Technical Parameters:
Max. Speed
21000rpm
Max. RCF
30910xg
Max. Capacity
4x800ml
Timer
0-99min
Speed Accuracy
±20rpm
Noise(DB)
≤65DBA
Voltage(V/HZ)
AC220V/110V,50HZ 10A
Dimension(LxWxHmm)
685x500x385mm
Net Weight(Kg)
70KG
Certificates
CE, ISO
Warranty
1 Year
TG18 High Speed/Low Speed Centrifuge Matched Rotors:
Order No.
Rotor Type
Max Speed(r/min)
Volume(ml)
Max. RCF(xg)
G18-1
Swing Rotor
4000
4x800ml
3450
G18-2
Microplate Rotor
4000
4x4x96well
2940
G18-3
Microplate Rotor
4000
2x4x96well
3210
G18-4
Microplate Rotor
4000
2x3x48well
2300
G18-5
Swing Rotor
4000
4x30x5ml vacuum tube
2840
G18-6
4x30x7ml vacuum tube
3140
G18-7
4x18x10ml vacuum tube
3140
G18-8
Swing Rotor
4000
Fat bottle
3830
G18-9
Fixed Rotor
16000
4x8PCR
15760
G18-10
Fixed Rotor
15000
6x8PCR
21420
G18-11
Fixed Rotor
16000
8x8PCR
17480
G18-12
Fixed Rotor
15000
12x8PCR
22930
G18-13
Fixed Rotor
15000
40×0.5ml
22920
G18-14
Fixed Rotor
21000
12×1.5/2ml
30910
G18-15
Fixed Rotor
16000
24×1.5/2ml
23440
G18-16
Fixed Rotor
14000
30×1.5/2ml
20800
G18-17
Fixed Rotor
13000
48×1.5/2ml
17930
G18-18
Fixed Rotor
16000
16x5ml
22020
G18-19
Fixed Rotor
16000
6x10ml
21500
G18-20
Fixed Rotor
15000
12x10ml
22680
G18-21
Fixed Rotor
13000
16x10ml
19490
G18-22
Fixed Rotor
13000
8x15ml
17790
G18-23
Fixed Rotor
11000
12x15ml
14330
G18-24
Fixed Rotor
5000
24x15ml
3500
G18-25
Fixed Rotor
5000
30x15ml
3830
G18-26
Fixed Rotor
14000
6x30ml
19060
G18-27
Fixed Rotor
13000
6x50ml(conical)
18840
G18-28
Fixed Rotor
13000
6x50ml(round)
18730
G18-29
Fixed Rotor
5000
12x50ml
3860
G18-30
Fixed Rotor
4000
24x50ml
2970
G18-31
Fixed Rotor
13000
4x85ml
18940
G18-32
Fixed Rotor
12000
4x100ml
14850
G18-33
Fixed Rotor
10000
6x100ml
11380
G18-34
Fixed Rotor
4000
12x100ml
2970
G18-35
Fixed Rotor
12000
24 capillaries
15800
G18-36
Swing Rotor
15000
4x5ml
19920
G18-37
Vertical Rotor
16000
16x5ml
16540
G18-38
Vertical Rotor
14000
8x30ml
19750
The Corners of our Company____________________________________
Not all cyanobacterial strains produce toxins. However, the toxin-producing strains cannot be distinguished from the nontoxin-producing strains by traditional light microscopy, commonlyused to monitor water bodies. An alternative for the differentiation of potentially toxic strains from nontoxic strains is to use molecular methods to detect the presence of toxin biosynthetic genes. Such methods are already available and could be used for the detection and identification of potential microcystin and nodularin producers present in environmental samples (Attogene catalog number NA2024).
Screening for the toxin itself, can be very costly. In turn, real time PCR for the detection of a gene region responsible for assembling in cyanobacterial strains and environmental samples can be a key indicator for the prescense of cyanobacteria capable of expressing the aetokthonotoxin toxin. Attogen has thus, designed primer pairs and probes targeting a the conserved gene region in order to enable the amplification and detection of several producer genera using real time PCR. Screening for the toxin genes can save significant costs and act as a triage for samples needing to be analyzed for the toxin itself.
Cyanobacterial neurotoxin aetokthonotoxin (AETX), a peculiar pentabrominated biindole alkaloid implicated in fatal Vacuolar Myelinopathy. This neurodegenerative disease was first recorded in 1994 during an outbreak of bald-eagle poisonings at De Gray Lake in Arkansas, USA. AETX was experimentally confirmed to be produced by the true branching heterocytous cyanobacterium Aetokthonos hydrillicola. The production of AETX is dependent on bromide (Br−) availability, and likely linked to its hyper-accumulation by the host plan. Thus regular monitoring of A. hydrillicola (accompanied by assessment of Br− and AETX levels) is highly advisable to predict the possible threat of further VM outbreaks.
The cyanobacterial AetA gene which encodes the unique FAD-dependent halogenase involved in the pathway for AETX synthesis has been adapted to develop a -aetokthonotoxin specific quantitative PCR (qPCR) assay.
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Real time qPCR kit for AetA gene For screening aetokthonotoxin gene cluster Use in combination with Attogene Algae DNA isolation kit