Inquiry

* Name

Phone

* Email

* Services or Products of Interest

Project Description

* Please note that all of our services and products are intended for preclinical research use only and cannot be used to diagnose, treat or manage patients.

* Tick to confirm the Research Use Only (RUO) statement.

Human S100A8 Baculovirus-Insect cells Overexpression Lysate

Inquiry

Specification

Cat. No.

NRT1005

Neurotransmitter Receptors, Transporters, and Ion Channels

S100A8

Product Type

Lysates

Product Name

Human S100A8 Baculovirus-Insect cells Overexpression Lysate

Size

300 µg

Price

Inquiry

Synonyms

Human 60B8AG Overexpression Lysate; Human CAGA Overexpression Lysate; Human CFAG Overexpression Lysate; Human CGLA Overexpression Lysate; Human CP-10 Overexpression Lysate; Human L1Ag Overexpression Lysate; Human MA387 Overexpression Lysate; Human MIF Overexpression Lysate; Human MRP-8 Overexpression Lysate; Human MRP8 Overexpression Lysate; Human NIF Overexpression Lysate; Human P8 Overexpression Lysate

Description

This Human S100A8 overexpression lysate was created in Baculovirus-Insect cells and intented for use as a Western blot (WB) positive control.

Species

Human

Molecule Mass

The recombinant human S100A8 consists of 103 amino acids and predicts a molecular mass of 12.2 kDa. It migrates as an approximately 14.6 kDa band 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

Baculovirus-Insect cells

Sequence Information

A DNA sequence encoding the human S100A8 (NP_002955.2) (Met 1-Glu 93) was expressed, fused with a polyhistidine tag at the C-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).

All of our services and products are intended for preclinical research use only and cannot be used to diagnose, treat or manage patients.