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Active Secondary Lymphoid Tissue Chemokine (SLC)
Active Secondary Lymphoid Tissue Chemokine (SLC)
CCL21; 6Ckine; CKb9; ECL; SCYA21; TCA4; ECL; Chemokine(C-C-Motif)Ligand 21; Beta Chemokine Exodus-2; Efficient Chemoattractant For Lymphocytes
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  • NO.:SBPB243Hu01
    Purity:>97%
    Applications:Cell culture, Activity Assays
    Organism Species:Homo sapiens (Human)
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Details

Buffer Formulation20mM Tris, 150mM NaCl, pH8.0, containing 1mM EDTA, 1mM DTT, 0.01% SKL, 5% Trehalose and Proclin300.
TraitsFreeze-dried powder
Purity> 97%
Isoelectric Point10.0
ApplicationsCell culture; Activity Assays.
ACTIVITY TEST

Secondary Lymphoid-tissue Chemokine (SLC) is a recently identified CC chemokine that is constitutively expressed in various lymphoid tissues and is a potent and specific chemoattractant for lymphocytes. Thus, chemotaxis assay used 24-well microchemotaxis system was undertaken to detect the chemotactic effect of SLC on the human T-lymphocyte leukemia cell line Jurkat. Briefly, Jurkat cells were seeded into the upper chambers (100uL cell suspension,106 cells/mL in RPMI 1640 with FBS free) and SLC (1ng/mL, 15ng/mL and 150ng/mL diluted separately in serum free RPMI 1640) was added in lower chamber with a polycarbonate filter (8um pore size) used to separate the two compartments. After incubation at 37℃ with 5% CO2 for 1h, the filter was removed, then cells in low chamber were observed by inverted microscope at low magnification (×100) and the number of migrated cells were counted at high magnification (×400) randomly (five fields for each filter). Result shows SLC is able to induce migration of Jurkat cells. The migrated Jurkat cells in low chamber at low magnification (×100) were shown in Figure 1. Five fields of each chamber were randomly chosen, and the migrated cells were counted at high magnification (×400). Statistical results were shown in Figure 2. The optimum chemotaxis of SLC occurs at 15-150ng/mL.(A)Jurkat cells were seeded into the upper chambers and serum free RPMI 1640 with 150ng/mL SLC was added in lower chamber, then cells in lower chamber were observed at low magnification (×100) after incubation for 1h;
(B)Jurkat cells were seeded into the upper chambers and serum free RPMI 1640 without SLC was added in lower chamber, then cells in lower chamber were observed at low magnification (×100) after incubation for 1h.
Figure. The chemotactic effect of SLC on Jurkat cells

Figure .The chemotactic effect of SLC on Jurkat cells.

 

USAGE

 

Reconstitute in 20mM Tris, 150mM NaCl (PH8.0) to a concentration of 0.1-1.0 mg/mL. Do not vortex.

 

STORAGE

 

Avoid repeated freeze/thaw cycles. Store at 2-8°C for one month. Aliquot and store at -80°C for 12 months.

 

STABILITY

 

The thermal stability is described by the loss rate. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37°C for 48h, and no obvious degradation and precipitation were observed. The loss rate is less than 5% within the expiration date under appropriate storage condition.

 



Image

Active Secondary Lymphoid Tissue Chemokine (SLC)
Figure. Gene Sequencing (Extract)

Image

APB575Hu01.png
Figure. SDS-PAGE

 

Active Secondary Lymphoid Tissue Chemokine (SLC)
Figure. Western Blot

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