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G5050

Sigma-Aldrich

Sephadex® G-50

Superfine

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About This Item

CAS Number:
9004-54-0
MDL number:
MFCD00132771
UNSPSC Code:
23151817
NACRES:
NA.56

form

powder

technique(s)

affinity chromatography: suitable

swelling

1 g swells to 9-11 mL

bead size

20-50 μm

pH

2—12

InChI

1S/C18H32O16/c19-1-5(21)9(23)10(24)6(22)3-31-17-16(30)14(28)12(26)8(34-17)4-32-18-15(29)13(27)11(25)7(2-20)33-18/h1,5-18,20-30H,2-4H2

InChI key

FZWBNHMXJMCXLU-UHFFFAOYSA-N

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General description

Sephadex® G-50 is a gel filtration medium used in affinity chromatography, protein chromatrography and gel filtration chromatography.
Fractionation Range (MW)
Globular Proteins: 1,500 - 30,000
Dextrans: 500 - 10,000

Application

Sephadex®G-50 has been used to purify the polymerase chain reaction (PCR) sequenced products.

Other Notes

G5050-100G′s updated product number is GE17-0041-01

Legal Information

Sephadex is a registered trademark of Cytiva

replaced by

Product No.
Description
Pricing

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Effect of probiotic treatment in broiler chicks on intestinal macrophage numbers and phagocytosis of Salmonella Enteritidis by abdominal exudate cells
Higgins SE, et al.
Poultry Science, 86(11), 2315-2321 (2007)
Matilde Marchi et al.
Epigenetics, 6(10), 1198-1206 (2011-09-21)
Leptin is a master regulator of energy homeostasis. Its expression, prevalently localized in adipocytes, is positively related to adipose mass. Epigenetics is emerging as an important contributor to the changes in gene expression undergone by adipose tissue during obesity. We
Vered Shkalim et al.
American journal of medical genetics. Part A, 149A(12), 2700-2705 (2009-11-19)
We present a family segregating for an autosomal dominant syndrome of hypotelorism, cleft palate/uvula, high-arched palate and mild mental retardation. Although these findings may suggest a form of holoprosencephaly, no holoprosencephaly was found on MRI of the proposita. Results of
Ilka Kleffner et al.
Journal of neurology, 257(11), 1864-1868 (2010-06-18)
Inherited neuropathies caused by mutations of the major structural protein of peripheral myelin, myelin protein zero (MPZ), contribute to 5% of all cases of Charcot-Marie-Tooth disease (CMT). They can be divided into an early-onset neuropathy with symptoms prior to the
M L Jirout et al.
Human molecular genetics, 19(13), 2567-2580 (2010-04-10)
Understanding catecholamine metabolism is crucial for elucidating the pathogenesis of hereditary hypertension. Here we integrated transcriptional and biochemical profiling with physiologic quantitative trait locus (eQTL and pQTL) mapping in adrenal glands of the HXB/BXH recombinant inbred (RI) strains, derived from
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