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SBP3500289

Sigma-Aldrich

RP105 Blocking Peptide for SAB3500289

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25 G
CN¥1,541.64
100 G
CN¥4,201.18

CN¥1,541.64


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25 G
CN¥1,541.64
100 G
CN¥4,201.18

About This Item

UNSPSC Code:
12352203
NACRES:
NA.41

CN¥1,541.64


In StockDetails


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biological source

synthetic

Quality Level

form

liquid

species reactivity

mouse, human

concentration

200 μg/mL

shipped in

wet ice

storage temp.

−20°C

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This Item
T12589334893328
assay

≥99.0% (NT)

assay

≥99.0% (titration)

assay

≥99.0% (NT)

assay

≥99.5% (NT)

product line

BioUltra

product line

-

product line

BioXtra

product line

BioUltra

Quality Level

300

Quality Level

300

Quality Level

200

Quality Level

100

form

crystalline powder

form

crystalline powder

form

crystalline powder

form

powder or crystals

solubility

H2O: 0.5 M at 20 °C, clear, colorless

solubility

water: 0.5 M, clear, colorless

solubility

H2O: 0.5 M at 20 °C, clear

solubility

H2O: 0.5 M at 20 °C, clear, colorless

pH

6.0-7.0 (25 °C, 0.5 M in H2O)

pH

6.0-7.0 (0.1 M in water, high purity)

pH

-

pH

3.0-4.5 (25 °C, 0.5 M in H2O)

Immunogen

14 amino acids near the carboxy terminus of human RP105.

Application

Used as a blocking peptide in immunoblotting applications.

Linkage

This peptide blocks the action of antibody SAB3500289.

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

Storage Class Code

10 - Combustible liquids

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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M Ito et al.
Life sciences, 38(12), 1089-1096 (1986-03-24)
[3H]L-glutamic acid binding to microfuge tubes and glass was investigated in four buffers. Background binding to these materials was negligible, but was increased by centrifugation or suction in Tris-HCl and Tris-citrate buffer. This binding was much less or eliminated when
Chi-Lin Li et al.
The Analyst, 137(22), 5222-5228 (2012-10-04)
Oligonucleotide (T30695) modified gold nanoparticles (T30695-Au NPs) have been prepared and employed for quantification of lead ions (Pb(2+)) in blood. The detection of Pb(2+) ions is through the formation of Au-Pb alloys and oligonucleotide-Pb(2+) complexes that catalyze the H(2)O(2)-mediated oxidation
Monica Cubillos-Rojas et al.
Methods in molecular biology (Clifton, N.J.), 869, 205-213 (2012-05-16)
Polyacrylamide gel electrophoresis (PAGE) is one of the most powerful tools used for protein analysis. We describe the use of Tris-acetate buffer and 3-15% polyacrylamide gradient gels to simultaneously separate proteins in the mass range of 10-500 kDa. We show
Patrick S Aranda et al.
Electrophoresis, 33(2), 366-369 (2012-01-10)
RNA-based applications requiring high-quality, non-degraded RNA are a foundational element of many research studies. As such, it is paramount that the integrity of experimental RNA is validated prior to cDNA synthesis or other downstream applications. In the absence of expensive
Monica Cubillos-Rojas et al.
Electrophoresis, 31(8), 1318-1321 (2010-03-24)
To separate and analyze giant and small proteins in the same electrophoresis gel, we have used a 3-15% polyacrylamide gradient gel containing 2.6% of the crosslinker bisacrylamide and 0.2 M of Tris-acetate buffer (pH 7.0). Samples were prepared in a

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