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Sigma-Aldrich

ColorBurst™ Electrophoresis Marker

mol wt 8,000-220,000 Da

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Synonym(s):
protein markers, protein molecular weight markers, protein standards
MDL number:
MFCD03456450
NACRES:
NA.25

form

solution

mol wt

8,000-220,000 Da

pH

8

shipped in

wet ice

storage temp.

−20°C

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Application

Brilliantly colored, exceptionally well-resolved, convenient, and stable, ColorBurst protein molecular weight markers perform impressively in a variety of gel compositions and concentrations. ColorBurst Markers are composed of 8 polypeptides which have been chemically reduced and conjugated to brilliantly colored dyes. Conveniently, ColorBurst Markers require no resuspension, reduction, or heating prior to use.
Colorburst can be used to estimate sample molecular weights, to monitor the progress of an electrophoretic run, or to confirm that an electroblot is complete.

Components

Solution contains myosin-violet, BSA-red, GDH-blue, ADH-red, Carbonic Anhydrase-orange, Trypsin Inhibitor-blue, Lysozyme-red, Aprotinin-blue, 200 mM Tris, SDS and, formamide. Each lot provides the apparent molecular weights determined by comparison to an unconjugated standard.

Quantity

Each vial of ColorBurst contains 500 μL of solution, enough for at least 50 mini gel applications.

Legal Information

ColorBurst is a trademark of Sigma-Aldrich Co. LLC

Pictograms

Health hazard
GHS08

Signal Word

Danger

Hazard Statements

H351 - H360D - H373

Hazard Classifications

Carc. 2 - Repr. 1B - STOT RE 2 Oral

Target Organs

Blood

Storage Class Code

6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 1

Regulatory Information

含少量动物源组分生物产品
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Meilyn Rodriguez-Hernandez et al.
Protein and peptide letters, 27(2), 145-157 (2019-10-18)
Glycogen storage disease type III (GSDIII, Cori/Forbes disease) is a metabolic disorder due to the deficiency of the Glycogen Debranching Enzyme (GDE), a large monomeric protein (about 176 kDa) with two distinct enzymatic activities: 4-α-glucantransferase and amylo-α-1,6-glucosidase. Several mutations along
Nidhi Nath et al.
International immunopharmacology, 88, 106925-106925 (2020-09-02)
Expression and single nucleotide polymorphisms (SNPs) of TLR4/9 and CYP1A1 genes are vital for cervical squamous cell carcinoma (CSCC) but considerably vary in different populations. A total of 255-subjects from Jharkhand (130-cases, 125-controls) were utilized to obtain the expression/SNP status
Yi-Shu Huang et al.
International journal of molecular sciences, 22(4) (2021-03-07)
Epidermal growth factor receptor (EGFR) specific therapeutics is of great importance in cancer treatment. Fcy-hEGF fusion protein, composed of yeast cytosine deaminase (Fcy) and human EGF (hEGF), is capable of binding to EGFR and enzymatically convert 5-fluorocytosine (5-FC) to 1000-fold
S V Demyanenko et al.
Molecular neurobiology, 57(7), 3219-3227 (2020-06-09)
Stroke is one of the leading reasons of human death. Ischemic penumbra that surrounds the stroke-induced infarction core is potentially salvageable, but molecular mechanisms of its formation are poorly known. Histone acetylation induces chromatin decondensation and stimulates gene expression. We
V A Dzreyan et al.
Molecular neurobiology, 58(1), 217-228 (2020-09-12)
Nerve injury is an important reason of human disability and death. We studied the role of histone deacetylation in the response of the dorsal root ganglion (DRG) cells to sciatic nerve transection. Sciatic nerve transection in the rat thigh induced
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