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Merck

D3287

Deoxyribonucleic acid, single stranded from human placenta

เข้าสู่ระบบ เพื่อดูราคาสำหรับองค์กรและสัญญา

เลือกขนาด

เปลี่ยนการดู

เกี่ยวกับสินค้านี้

CASE番号:
UNSPSC Code:
12352200
MDL number:
eCl@ss:
32160414
Form:
solution
Solubility:
water: 9-12 mg/mL
Storage temp.:
−20°C
บริการทางเทคนิค
ต้องการความช่วยเหลือหรือไม่ ทีมนักวิทยาศาสตร์ที่มีประสบการณ์ของเราอยู่ที่นี่เพื่อคุณ
ให้เราช่วยเหลือ


grade

Molecular Biology

description

For hybridization

form

solution

mol wt

(Fragments from 587-831 bp.)

solubility

water: 9-12 mg/mL

storage temp.

−20°C

InChI

1S/C15H31N3O13P2/c16-13-1-7(20)11(28-13)5-25-32(21,22)31-9-3-15(18)29-12(9)6-26-33(23,24)30-8-2-14(17)27-10(8)4-19/h7-15,19-20H,1-6,16-18H2,(H,21,22)(H,23,24)

InChI key

AWBASQCACWFTGD-UHFFFAOYSA-N

General description

Human placental DNA is isolated from donor placenta, but will contain some maternal DNA. The DNA fragments are sonicated to produce fragments of consistent size.

Application

Many factors contribute to the signal-to-noise ratio in nucleic acid hybridizations. These factors include the presence of solvent (formamide), hybridization temperature, length of hybridization, volume of hybridization solution, degree and method of agitation, use of blocking reagents, concentration and specific activity of the probe, use of molecular agents to increase the rate of nucleic acid reassociation, and the degree of stringency used during the washing of the membrane.

In order to decrease any non-specific hybridization of the probe to a substrate, blocking agents must be used. Generally, a combination of blocking reagent, detergent, and denatured, fragmented DNA is used to accomplish this. Sigma offers sonicated, denatured DNA from a variety of species for use as a blocking agent in Northern and Southern blotting and other nucleic acid hybridization techniques.
Sonicated Deoxyribonucleic acid, single stranded from human placenta, was used as blocking agent in Southern hybridization of DNA from human papillomavirus (HPV) positive SiHa, HeLa and CaSki cell-lines. It was used as standard in GC/MS analysis of exocyclic DNA adducts.

Features and Benefits

• High quality human DNA.
• DNA fragments of defined sizes.

Other Notes

DNA is supplied in a solution of 100mM phosphate buffer.  This is a ready to use concentrated solution
of 9-12 mg/ml DNA in 100mM phosphate buffer. However, it will reanneal on standing at room temperature so it is recommended to boil the solution for 10 minutes and then cool on ice for at least 5 minutes prior to use. Cooling on ice will
reduce the chances for reannealing, as it is more likely to reanneal if cooled at room temperature.


คลาสการจัดเก็บ

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)



เลือกจากเวอร์ชันล่าสุด:

ใบรับรองผลการวิเคราะห์ (COA)

หมายเลขล็อต/ชุด

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ดูห้องสมุดเอกสาร


เนื้อหาที่เกี่ยวข้อง


Mark F Evans et al.
BMC clinical pathology, 3(1), 2-2 (2003-06-13)
BACKGROUND: Over the past five years in situ hybridization techniques employing tyramide amplification reagents have been developed and promise the potential detection of low/single-copy nucleic acid sequences. However the increased sensitivity that tyramide amplification brings about may also lead to
H J Chen et al.
Chemical research in toxicology, 12(12), 1119-1126 (1999-12-22)
Exocyclic DNA adducts have been reported to derive from various exogenous as well as endogenous sources, such as lipid peroxidation. Among them, 1,N(6)-ethenoadenine (epsilonAde) has previously been detected in tissue DNA of untreated rodents and humans by an immunoaffinity/(32)P-postlabeling method.
Asife Sahinarslan et al.
Acta cardiologica, 68(3), 291-297 (2013-07-26)
Both computed tomography (CTA) and conventional angiography (CCA) can provide direct visualization of the coronary arteries. The aim of the present study was to compare the radiation exposure between CTA and CCA and to search whether this amount of radiation