Human NRG1 Beta 1 HEK293 Overexpression Lysate

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Human NRG1 Beta 1 HEK293 Overexpression Lysate

Specification
Cat. No.
NSC679
Category
Neural Stem Cell Growth Factors
Product Type
Lysates
Product Name
Human NRG1 Beta 1 HEK293 Overexpression Lysate
Size
300 µg
Price
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Synonyms
Human ARIA Overexpression Lysate; Human GGF Overexpression Lysate; Human GGF2 Overexpression Lysate; Human HGL Overexpression Lysate; Human HRG Overexpression Lysate; Human HRG1 Overexpression Lysate; Human HRGA Overexpression Lysate; Human MST131 Overexpression Lysate; Human MSTP131 Overexpression Lysate; Human NDF Overexpression Lysate; Human Neuregulin 1 Overexpression Lysate; Human NRG1-IT2 Overexpression Lysate; Human SMDF Overexpression Lysate
Species
Human
Molecule Mass
The recombinant human NRG1(aa2-246)/Fc chimera is a disulfide-linked homodimeric protein. The reduced monomer consists of 505 amino acids and has a calculated molecular mass of 55.2 kDa. In SDS-PAGE under reducing conditions, the apparent molecular mass of the protein is approximately 75 kDa due to glycosylation.
Stability & Storage
Store at 4℃ for up to twelve months from date of receipt. After re-dissolution, aliquot and store at -80℃ for up to twelve months. Avoid repeated freeze-thaw cycles.
Product Description
This Human Neuregulin-1/NRG1 overexpression lysate was created in HEK293 Cells and intented for use as a Western blot (WB) positive control. Purification of Neuregulin-1/NRG1 protein (Cat: 11609-H01H2) from the overexpression lysate was verified.
Expression Host
HEK293 Cells
Sequence Information
A DNA sequence encoding the N-terminal fragment (Ser 2-Lys 246) of human NRG1 isoform beta1 (Q02297-6) was fused with the Fc region of human IgG1 at the N-terminus.
Preparation Method
Cell lysate was prepared by homogenization of the over-expressed cells in ice-cold modified RIPA Lysis Buffer with cocktail of protease inhibitors (Sigma). Cell debris was removed by centrifugation. Protein concentration was determined by Bradford assay (Bio-Rad protein assay, Microplate Standard assay). The cell lysate was boiled for 5 min in 1 x SDS loading buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1% sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% b-mercaptoethanol, and lyophilized.
Lysis Buffer
Modified RIPA Lysis Buffer: 50 mM Tris-HCl pH 7.4, 150 mM NaCl, 1mM EDTA, 1% Triton X-100, 0.1% SDS, 1% Sodium deoxycholate, 1mM PMSF.
Recommend Usage
1.  Centrifuge the tube for a few seconds and ensure the pellet at the bottom of the tube. 2.  Re-dissolve the pellet using 200μL pure water and boil for 2-5 min.
Sample Buffer
1 X Sample Buffer (1 X modified RIPA buffer+1 X SDS loading buffer).
Application
Western Blot (WB)Optimal dilutions/concentrations should be determined by the end user.
All of our services and products are intended for preclinical research use only and cannot be used to diagnose, treat or manage patients.

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