Goat Anti-XCL1 / XCL2 Antibody

Supplied at 0.5 mg/ml in Tris saline, 0.02% sodium azide, pH7.3 with 0.5% bovine serum albumin.

100 µg

Aliquot and store at -20°C. Minimize freezing and thawing.

XCL1|chemokine (C motif) ligand 1|ATAC|LPTN|LTN|SCM-1|SCM-1a|SCM1|SCYC1|OTTHUMP00000032498|OTTHUMP00000060404|lymphotactin|region containing small inducible cytokine subfamily C, member 1 (lymphotactin)|small inducible cytokine subfamily C, member 1 (lymphotactin)|small inducible cytokine subfamily C, member 1 (lymphotactin)|small inducible cytokine subfamily C, member 2|small inducible cytokine subfamily C, member 1 (lymphotactin)

NP_002986.1; NP_003166.1

EBP09195

Peptide with sequence C-RDVVRSMDRKSNTRN, from the internal region of the protein sequence according to NP_002986.1; NP_003166.1.

XCL1 and CXL2 are almost identical and therefore this antibody is expected to recognize both proteins.

C-RDVVRSMDRKSNTRN

Purified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide.

Refrigerated

Human

6375

Antibody detection limit dilution 1:16000.

Preliminary experiments gave an approx 80kDa band in Human Peripheral Blood Mononucleocytes lysates after 0.3µg/ml antibody staining. Please note that currently we cannot find an explanation in the literature for the band we observe given the calculated size of 12.5kDa according to NP_002986.1 and 12.6kDa according to 003166.1. The 80kDa band was successfully blocked by incubation with the immunizing peptide. We would appreciate any feedback from people in the field - have any results been reported with other antibodies/lysates? Have any further splice variants/modified forms been reported?

Pep-ELISA