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Merck
CN

63036

氯化镁 溶液

BioUltra, Molecular Biology, ~0.025 M in H2O

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线性分子式:
MgCl2
化学文摘社编号:
7786-30-3
分子量:
95.21
NACRES:
NA.26
PubChem Substance ID:
329759763
UNSPSC Code:
12352302
MDL number:
MFCD00011106
Grade:
Molecular Biology

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cation traces

Cu: ≤1 mg/kg, Al: ≤1 mg/kg, As: ≤0.1 mg/kg, Ba: ≤1 mg/kg, Bi: ≤1 mg/kg, Ca: ≤10 mg/kg, Cd: ≤1 mg/kg, Co: ≤1 mg/kg, Cr: ≤1 mg/kg, Fe: ≤1 mg/kg, K: ≤500 mg/kg, Li: ≤1 mg/kg, Mn: ≤1 mg/kg, Mo: ≤1 mg/kg, Na: ≤1000 mg/kg, Ni: ≤1 mg/kg, Pb: ≤1 mg/kg, Sr: ≤1 mg/kg, Zn: ≤1 mg/kg

InChI

1S/2ClH.Mg/h2*1H;/q;;+2/p-2

InChI key

TWRXJAOTZQYOKJ-UHFFFAOYSA-L

grade

Molecular Biology

product line

BioUltra

concentration

~0.025 M in H2O

impurities

DNases, none detected, RNases, none detected, insoluble matter, passes filter test, phosphatases, none detected, proteases, none detected, ≤0.0002% total nitrogen (N)

pH

5.0-7.0 (25 °C)

anion traces

phosphate (PO43-): ≤5 mg/kg, sulfate (SO42-): ≤20 mg/kg

λ

neat

UV absorption

λ: 260 nm Amax: 0.03, λ: 280 nm Amax: 0.03

Quality Level

100

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Packaging

package of 10 × 1 mL ampouls

存储类别

10 - Combustible liquids

wgk

nwg

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCCG6475
BCBT8379

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Brain tumor pathology, 32(1), 22-30 (2014-04-22)
Assessment of the mutational status of the isocitrate dehydrogenase 1/2 (IDH1/2) gene has become an integral part of the standard diagnostic procedure and, therefore, needs to be accurate. This may, however, be compromised by various factors including the method of
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Human molecular genetics, 23(13), 3579-3595 (2014-02-20)
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Susanne Hellmuth et al.
The EMBO journal, 33(10), 1134-1147 (2014-05-02)
The universal triggering event of eukaryotic chromosome segregation is cleavage of centromeric cohesin by separase. Prior to anaphase, most separase is kept inactive by association with securin. Protein phosphatase 2A (PP2A) constitutes another binding partner of human separase, but the
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PLoS genetics, 10(7), e1004494-e1004494 (2014-08-01)
Exome sequencing studies in complex diseases are challenged by the allelic heterogeneity, large number and modest effect sizes of associated variants on disease risk and the presence of large numbers of neutral variants, even in phenotypically relevant genes. Isolated populations
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