R8759

Ribonucleic acid, transfer from baker′s yeast (S. cerevisiae)

Name: Ribonucleic acid, transfer from baker′s yeast (<I>S. cerevisiae</I>)
Brand: SIGMA
Price: 341 PLN

Type X-SA, lyophilized powder

Synonym(s):

Transfer RNA, tRNA

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100 UNITS

PLN 341.00

500 UNITS

PLN 943.50

2000 UNITS

PLN 3,080.00

10000 UNITS

PLN 11,120.00

PLN 341.00

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About This Item

CAS Number:

9014-25-9

UNSPSC Code:

41106305

NACRES:

NA.51

MDL number:

MFCD00132200

Key Documents

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Product Name

Ribonucleic acid, transfer from baker′s yeast (S. cerevisiae), Type X-SA, lyophilized powder

type

Type X-SA

form

lyophilized powder

Quality Level

200

color

white to off-white

solubility

water: 10 mg/mL, clear to slightly hazy, colorless to light yellow

storage temp.

−20°C

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Biochemicals

Nucleosides and Nucleotides

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Show Differences

1 of 4

This Item	R5636	R4752	R8508
Sigma-Aldrich R8759 Ribonucleic acid, transfer from baker′s yeast (S. cerevisiae)	Sigma-Aldrich R5636 Ribonucleic acid, transfer from baker′s yeast (S. cerevisiae)	Sigma-Aldrich R4752 Ribonucleic acid, transfer from bovine liver	Sigma-Aldrich R8508 Ribonucleic acid, transfer from baker′s yeast (S. cerevisiae)
Quality Level 200	Quality Level 200	Quality Level 200	Quality Level 200
form lyophilized powder	form buffered aqueous solution	form lyophilized powder	form buffered aqueous solution
storage temp. −20°C	storage temp. −20°C	storage temp. −20°C	storage temp. −20°C
type Type X-SA	type -	type Type XI	type -

Application

Ribonucleic acid, transfer from baker′s yeast S. cerevisiae may be used as a starting material for the purification of specific amino acyl-tRNA species by methods such as liquid column chromatography or high-performance liquid chromatography (HPLC).

Other Notes

One unit will yield an A₂₆₀ of 1.0 in 1.0 mL of water (1 cm light path).

Preparation Note

Prepared by a modification of the procedure of Hancher, C.W., et al., Biotechnol. Bioeng., 11, 1055 (1969).

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Pseudouridine-mediated translation control of mRNA by methionine aminoacyl tRNA synthetase.

Ofri Levi et al.

Nucleic acids research, 49(1), 432-443 (2020-12-12)

Modification of nucleotides within an mRNA emerges as a key path for gene expression regulation. Pseudouridine is one of the most common RNA modifications; however, only a few mRNA modifiers have been identified to date, and no one mRNA pseudouridine

A new method to remove hybridization bias for interspecies comparison of global gene expression profiles uncovers an association between mRNA sequence divergence and differential gene expression in Xenopus.

Maureen A Sartor et al.

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The recent sequencing of a large number of Xenopus tropicalis expressed sequences has allowed development of a high-throughput approach to study Xenopus global RNA gene expression. We examined the global gene expression similarities and differences between the historically significant Xenopus

Satellite DNA-containing gigantic introns in a unique gene expression program during Drosophila spermatogenesis.

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Intron gigantism, where genes contain megabase-sized introns, is observed across species, yet little is known about its purpose or regulation. Here we identify a unique gene expression program utilized for the proper expression of genes with intron gigantism. We find

The Wnt pathway limits BMP signaling outside of the germline stem cell niche in Drosophila ovaries.

Violaine I Mottier-Pavie et al.

Developmental biology, 417(1), 50-62 (2016-07-02)

The mechanisms that modulate and limit the signaling output of adult stem cell niches remain poorly understood. To gain further insights into how these microenvironments are regulated in vivo, we performed a candidate gene screen designed to identify factors that

Gradients of Eph-A6 expression in primate retina suggest roles in both vascular and axon guidance.

Peter Kozulin et al.

Molecular vision, 15, 2649-2662 (2009-12-17)

Recently we identified high levels of expression of Eph-A6 in the macula of developing human retina and showed localization of Eph-A6 to ganglion cells (GC). In the present study we investigated the expression of some members of the ephrin family

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Ribonucleic acid, transfer from baker′s yeast (S. cerevisiae)