CD68 Blocking Peptide for STJ500482 peptide (STJ505605)

SPECIFICATIONS
ImmunogenSynthetic peptide taken within amino acid region 240-290 on mouse CD68/Macrosialin protein.
STJ505605-250
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General Information

Short DescriptionCD68 Blocking Peptide for STJ500482 is synthetically produced from the 240-290 sequence and is suitable for use in western blot applications.
ApplicationsImmunodepletion/Immunocompetition
NoteSTRICTLY FOR FURTHER SCIENTIFIC RESEARCH USE ONLY (RUO). MUST NOT TO BE USED IN DIAGNOSTIC OR THERAPEUTIC APPLICATIONS.

Product Properties

FormulationLiquid form at 2.5mg/ml concentration in PBS. Up to 5% DMSO can be added. Orders with >1mg can be supplied in lyophilized powder form, or in buffer of choice.
Storage InstructionStore at-20°C for long term storage. Avoid freeze-thaw cycles.

Target Information

Gene SymbolCd68
Gene ID12514
Uniprot IDCD68_MOUSE
ImmunogenSynthetic peptide taken within amino acid region 240-290 on mouse CD68/Macrosialin protein.
Immunogen Region240-290
SpecificityThis blocking peptide is recommended for use in combination with CD68 antibody, STJ500482

Additional Info

Tissue Specificity Expressed in tissue macrophages and to a lesser extent in dendritic cells.
Post Translational Modifications N- and O-glycosylated.
Function Could play a role in phagocytic activities of tissue macrophages, both in intracellular lysosomal metabolism and extracellular cell-cell and cell-pathogen interactions. Binds to tissue- and organ-specific lectins or selectins, allowing homing of macrophage subsets to particular sites. Rapid recirculation of CD68 from endosomes and lysosomes to the plasma membrane may allow macrophages to crawl over selectin-bearing substrates or other cells.
Peptide Name Macrosialin
Cd Antigen Cd68
Database Links Reactome: R-MMU-6798695
Cellular Localisation Isoform Long: Endosome Membrane
Single-Pass Type I Membrane Protein
Lysosome Membrane
Isoform Short: Cell Membrane
Alternative Peptide Names Macrosialin protein
Cd Antigen Cd68 protein
Cd68 protein

Information sourced from Uniprot.org

Citations

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