Vivantis Technologies Sdn Bhd

  • Increase font size
  • Default font size
  • Decrease font size

Chromatein Prestained Protein Ladder

Description
Chromatein Prestained Protein Ladder contains 11 proteins that resolve into sharp, tight bands in the range of 10-175 kDa. It is supplied in a loading buffer for direct loading on gels. Allows monitoring molecular weight separation during electrophoresis, estimation of molecular weights of interest and evaluate western transfer efficiency.

Feature
Broad Range: 10-175kDa
Convenient: Supplied in a loading buffer for direct loading
Easy Identification: ~10, ~40, and ~90kDa reference bands coupled with a blue dye

Quality Control
Tested in SDS-polyacrylamide gel electrophoresis and western blotting

Storage

  • Stable at 4°C for 3 months
  • Store at -20°C for 24 months

 

Ordering Information

Catalog No Description Pack Size
PR0602 Chromatein Prestained Protein Ladder (ready-to-use) (Sell while stock last) 2 x 250 μl

Download
Manual

Chromatein Prestained Protein Ladder

Download
MSDS

Chromatein Prestained Protein Ladder

Publication

This Product Has Been Used In:

Ng Y.K. et al. (2022) Characterization of Sphingobacterium sp. Ab3 Lipase and Its Coexpression with LEA Peptides. Microbiology Spectrum. DOI: https://doi.org/10.1128/spectrum.01422-21

Mayahi V, Esmaelizad M & Harzandi N (2018) Designing a Novel Recombinant HN Protein with Multi Neutralizing Antigenic Sites and Auto Tag Removal Ability Based on NDV-VIIj for Diagnosis and Vaccination Application, Indian Journal of Microbiology58(3):326-331.

Dehnaiv, E., Fathi-Roudsari,M., Mirzaie, S., Arab., S.S., Siadat, S.O.R., Khajeh, K. (2017) Engineering disulfide bonds in Selenomonas ruminantium B-xylosidase by experimental and computational methods. International Journal of Biological Macromolecules. 95. Pp.248-255

Karimi, M., Biria, D. (2016) ) The synergetic effect of starch and alpha amylase on the biodegradation of n-alkanes

Golshani, M., et al. (2016) In silico Analysis of Brucella abortus 0mp2b and In vitro Expression of S0mp2b. Clinical and Experimental Vaccine Research. 5(1), p.75-82.

Golshani, M., Rafati, S., Siadat, S.D.,Nejati-Moheimani, M., Shahcheraghi, F., Arsang, A., Bouzari, S. (2015) Improved immunogenicity and protective efficacy of a divalent DNA vaccine encoding Brucella L7/L12-truncated Omp31 fusion protein by a DNA priming and protein boosting regimen. Molecular Immunology 66. Pp.384-391.

Ungcharoenwiwat, P., H-Kittikun A. (2015) Purification and characterization of lipase from Burkholderia sp. EQ3 isolated from wastewater from a canned fish factory and its application for the synthesis of wax esters. Journal of Molecular Catalysis B: Enzymatic.115. Pp..96-104

Thongsaiklaing, T., et al. (2014)Analysis of the α-amylase Gene Sequence and the Enzyme Activity of Indian Rock Oyster Saccostrea forskali . Fisheries ScienceProQuest. p. 589-601.

Gharajelar, S.N., Ahmadi, M., & Hosseini, B. (2012) 2015) Cloning and Expression of the Immunogenic Moiety of Pseudomonas aeruginosa Exotoxin A Biological Journal of Microorganism1(4), p. 7-14.

 

DOWNLOAD & RESOURCES

Brochure
MSDS
Video
Promotion

 

ADDITIONAL INFORMATION

ISO Certificate
RE Buffers Activity Chart

Reaching Us

Headquarters

Vivantis Technologies Sdn Bhd

Revongen Corporation Center,

Level 17, Top Glove Tower,

No. 16, Persiaran Setia Dagang,

Setia Alam, Seksyen U13,

40170 Shah Alam,

Selangor Darul Ehsan,

Malaysia.


Tel: +603-3359 1166

Fax: +603-3358 0303

 

 

ACCOLADES & ACCREDITATION

Acquaint Us

International Distribution/OEM services:

Email: international@vivantechnologies.com

WhatsApp: +6012 793 0184


Local Distribution/Sales Inquiries:

Email: info@vivantechnologies.com

WhatsApp: +6016 216 0492


Product Technical Support:

vivalab@vivantechnologies.com


General Enquiries:

info@vivantechnologies.com

 

SOCIAL MEDIA