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Chemokines / cytokines

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Pull down assay of GTX65634-pro CD137L protein (DDDDK tagged) by hCD137-Fc. 1. hCD137-Fc + hCD137L-DDDDDK-tag 2. hCD137-Fc + hGITRL-DDDDDK-tag 3. hCD137-Fc + hGITRL-His-tag 4. hGITR-Fc + hCD137L-DDDDDK-tag 5. hGITR-Fc + hGITRL-DDDDDK-tag
Product group Proteins / Signaling Molecules
GeneTex
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GTX65635-pro CD40L protein (multimeric) does not need an enhancer to induce B cells activation. Method: PBL cells were incubated in 96-well plates (2x105 cells/well in 100microl RPMI supplemented with 10% FCS) for 24 hours at 37oC with the indicated concentration of CD40L (multimeric) or CD40L in the presence and absence of 1microg/ml Enhancer. Cells were washed with PBS and stained with CD86-PE antibody and CD19-FITC antibody, and then analyzed by flow cytometry.
Product group Proteins / Signaling Molecules
GeneTex
ApplicationsFunctional Assay
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Deglycosylation of GTX65638-pro rat progranulin (DDDDK tagged) protein. To examine the deglycosylation of rat Progranulin (DDDDDK tagged), 1 microg of rat progranulin is denatured with 1X glycoprotein denaturing buffer at 100oC for 10 minutes. After the addition of NP-40 and G7 reaction buffer, twofold dilutions of PNGase F are added and the reaction mix is incubated for 1 or 3 hours at 37oC. Separation of reaction products is visualized by immunoblotting using anti-DDDDDK-HRP antibody.
Product group Proteins / Signaling Molecules
GeneTex
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The effects on phospho-ERK1/2 and ERK1/2 by GTX65641-pro Progranulin protein in neuronal differentiated mouse P19 cells. Undifferentiated mouse P19 cells were induced to differentiated in 1microM retinoic acid (RA) in alpha-minimum essential medium (alphaMEM) containing 10% heat-treated fetal bovine serum on bacterial grade plates for 3~4 days to allow aggregates to form (generation of embryonic bodies). The aggregates were then plated on tissue culture grade plates in the absence of RA for 3~4days. To examine the induction of signal of phospho-ERK1/2 and ERK1/2, reactions were carried out at 37oC over 0, 5, 10, 30, 60, 120mins, respectively by adding the recombinant protein (500ng/ml) to the neuronal differentiated mouse P19 cells, which were maintained with serum starvation for 24hrs. Treatment with Progranulin protein (GTX65641-pro) was performed in lanes 1, 2, 3, 4, 5, and 6 over 0, 5, 10, 30, 60, 120mins, respectively. GAPDH was used as loading control for western blotting.
Product group Proteins / Signaling Molecules
GeneTex
ApplicationsFunctional Assay
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Deglycosylation of GTX65642-pro Progranulin (mouse) protein.To examine the deglycosylation of mouse Progranulin, 1 microg of mouse progranulin is denatured with 1X glycoprotein denaturing buffer at 100oC for 10 minutes. After the addition of NP-40 and G7 reaction buffer, two fold dilutions of PNGase F are added and the reaction mix is incubated for 1 hour at 37oC. Separation of reaction products is visualized by immunoblotting using anti-Progranulin (mouse) antibody.
Product group Proteins / Signaling Molecules
GeneTex
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Product group Proteins / Signaling Molecules
GeneTex
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Product group Proteins / Signaling Molecules
GeneTex
Protein IDP10749
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Product group Proteins / Signaling Molecules
GeneTex
ApplicationsFunctional Assay
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Product group Proteins / Signaling Molecules
GeneTex
ApplicationsFunctional Assay
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Product group Proteins / Signaling Molecules
GeneTex
ApplicationsFunctional Assay
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Product group Proteins / Signaling Molecules
GeneTex
ApplicationsFunctional Assay
  • SizePrice
Product group Proteins / Signaling Molecules
GeneTex
ApplicationsFunctional Assay
  • SizePrice