Human S100A4 HEK293 Overexpression Lysate

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Human S100A4 HEK293 Overexpression Lysate

Specification
Cat. No.
NRT1001
Neurotransmitter Receptors, Transporters, and Ion Channels
S100A4
Product Type
Lysates
Product Name
Human S100A4 HEK293 Overexpression Lysate
Size
300 µg
Price
Inquiry
Synonyms
Human 18A2 Overexpression Lysate; Human 42A Overexpression Lysate; Human CAPL Overexpression Lysate; Human FSP1 Overexpression Lysate; Human MTS1 Overexpression Lysate; Human P9KA Overexpression Lysate; Human PEL98 Overexpression Lysate
Description
This Human S100A4 overexpression lysate was created in HEK293 Cells and intented for use as a Western blot (WB) positive control.
Species
Human
Molecule Mass
The recombinant human Fc/S100A4 is a disulfide-linked homodimeric protein. The reduced monomer consists of 338 amino acids and has a predicted molecular mass of 38.4 kDa. As a result of glycosylation, the apparent molecular mass of rhFc/S100A4 monomer is approximately 40 kDa in SDS-PAGE under reducing conditions.
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.
Application
Western Blot (WB). Optimal dilutions/concentrations should be determined by the end user.
Expression Host
HEK293 Cells
Sequence Information
A DNA sequence encoding the human S100A4 (NP_002952.1) (Met 1-Lys 101) was expressed with the fused 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).
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