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Human CCL21/6Ckine MAb (Clone 54111) (500 UG)

货号: MAB3661 基本售价: 5026.6 元 规格: 500 ug

产品信息

概述
货号MAB3661
描述For ELISA the Antibody Pairs information:Capture antibody:MAB3661;Detection antibody:BAF366; and protein: 366-6C-025
别名6Ckine; 6CkineSmall-inducible cytokine A21; Beta-chemokine exodus-2; chemokine (C-C motif) ligand 21; CKb9; exodus-2; member 21; SCYA21; SCYA21MGC34555; secondary lymphoid tissue chemokine; SLC; SLCSecondary lymphoid-tissue chemokine; TCA-4
反应种属Human
应用Western Blot(1 µg/mL)
ELISA Capture (Matched Antibody Pair)(2-8 µg/mL )
ELISA Detection (Matched Antibody Pair)(0.1-0.4 µg/mL )
ELISA Standard ( )
目标/特异性Detects human CCL21/6Ckine in ELISAs and Western blots. In Western blots, shows 100% cross-reactivity with recombinant human (rh) CCL24. Under reducing conditions, shows approximately 10-50% cross-reactivity with rhCCL2, 8, 13, 28, and rmCCL2. Does not
cross-react with rhCCL1, 3, 4, 5, 7, 9, 11, 14a, 15, 17, 18, 19, 20, 22, 23, 25, rmCCL1, 3, 4, 6, 7, 9, 11, 12, 19, 20, 21, 22, 24, 25, 28, or rrCCL20.
使用方法Western Blot: 1 µg/mL
ELISA Capture (Matched Antibody Pair): 2-8 µg/mL 
ELISA Detection (Matched Antibody Pair): 0.1-0.4 µg/mL 
ELISA Standard :  
来源Reconstitute at 0.5 mg/mL in sterile PBS.
产品组分
性能
供应商R&D Systems
Entrez Gene IDs6366 (Human); 18829 (Mouse); 298006 (Rat)
应用文献
R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.

Lymph node chemokines promote sustained T lymphocyte motility without triggering stable integrin adhesiveness in the absence of shear forces.
Authors: Woolf E, Grigorova I, Sagiv A, Grabovsky V, Feigelson SW, Shulman Z, Hartmann T, Sixt M, Cyster JG, Alon R
Nat. Immunol., 2007;8(10):1076-85.
Species: Human
Sample Type: Whole Cells
Application: Neut

纯化方式Protein A or G purified from hybridoma culture supernatant
免疫原E. coli-derived recombinant human CCL21/6Ckine
Ser24-Pro134
Accession # O00585
生物活性Human
标记Unconjugated
溶解方法Reconstitute at 0.5 mg/mL in sterile PBS.
背景

6Ckine is a novel CC chemokine discovered independently by three groups from the EST database. 6Ckine, also named SLC (Secondary Lymphoid-tissue Chemokine), CCL21 and Exodus-2, shows 21 - 33% identity to other CC chemokines. 6Ckine contains the four conserved cysteines characteristic of beta chemokines plus two additional cysteines in its unusually long carboxyl-terminal domain. Human 6Ckine cDNA encodes a 134 amino acid residue, highly basic, precursor protein with a 23 amino acid residue signal peptide that is cleaved to form the predicted 111 amino acid residue mature protein. Mouse 6Ckine cDNA encodes a 133 amino acid residue protein with a 23 residue signal peptide that is cleaved to generate the 110 residue mature protein. Human and mouse 6Ckine are highly conserved, exhibiting 86% amino acid sequence identity. 6Ckine is constitutively expressed at high levels in lymphoid tissues such as lymph nodes, spleen and appendix. In mouse, high levels of 6Ckine mRNA are also detected in the lung. The gene for human 6Ckine has been localized at human chromosome 9p13 rather than chromosome 17 where the genes of many human CC chemokines are clustered. The 6Ckine gene location is within a region of about 100 kb from the gene for
MIP‑3 beta /ELC, another novel CC chemokine. Unlike most CC chemokines, 6Ckine is not chemotactic for monocytes. Recombinant mouse 6Ckine is chemotactic in vitro for thymocytes and activated T cells. Recombinant human 6Ckine has been shown to be chemotactic for some human T cell lines, resting PBL, and cultured T cells expanded with PHA and IL-2. 6Ckine has also been reported to inhibit hemopoietic progenitor colony formation in a dose-dependent manner. 6Ckine acts via a class of as yet unidentified CC receptors on both T cells and B cells that are not shared by any other CC chemokines so far tested.

运输条件Blue Ice
存放说明-20℃
参考文献
  1. Hedrick, J.A. and A. Zlotnik (1997) J. Immunol. 159:1589.
  2. Hromas, R. et al. (1997) J. Immunol. 159:2554.
  3. Nagira, M. et al. (1997) J. Biol. Chem. 272:19518.