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Recombinant Rabbit Anti-PRF1 Monoclonal Antibody
Recombinant Rabbit Anti-PRF1 Monoclonal Antibody
HPLH2; P1; PFP; Pfn; Prf-1; Cyta; RATCYTA; PERF_HUMAN; PRF1; Cytolysin; Lymphocyte pore-forming protein (PFP); PERF_MOUSE; Lymphocyte pore-forming protein; PERF_RAT; perforin 1; perforin 1 (pore forming protein); Perforin; perforin 1 (preforming protein);
Total $295.0
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  • NO.:SLA0453M
    concentration:1mg/ml
    React Species:Human
    Immunogen Species:Mouse
    Clonality:Monoclonal
    Applications:WB, IHC-P, IHC-F, IF, ELISA
    Gene name:PRF1
    UniProt Entry:P14222
    NCBI Gene Entry:5551
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Product NameRecombinant Rabbit Anti-PRF1 Monoclonal Antibody
Cat No.SLA0453M
Chinese Name穿孔素单克隆抗体
AliasHPLH2; P1; PFP; Pfn; Prf-1; Cyta; RATCYTA; PERF_HUMAN; PRF1; Cytolysin; Lymphocyte pore-forming protein (PFP); PERF_MOUSE; Lymphocyte pore-forming protein; PERF_RAT; perforin 1; perforin 1 (pore forming protein); Perforin; perforin 1 (preforming protein);
Host SpeciesMouse
ClonalityMonoclonal
Clone No.3C3
React SpeciesHuman
ApplicationsWB (1:500-2000)
IHC-P (1:100-500)
IHC-F (1:100-500)
IF (1:100-500)
ELISA (1:5000-10000)
Not yet tested in other applications.
Optimal working dilutions must be determined by the end user.
ImmunogenKLH conjugated synthetic peptide derived from human Perforin
Purificationaffinity purified by Protein A
Concentration1mg/ml
Predicted MW.59 kDa
Subcellular LocationCytoplasm
Gene ID5551
Swiss-ProtP14222
Storage0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
BackgroundThe protein encoded by this gene has structural and functional similarities to complement component 9 (C9). Like C9, this protein creates transmembrane tubules and is capable of lysing non-specifically a variety of target cells. This protein is one of the main cytolytic proteins of cytolytic granules, and it is known to be a key effector molecule for T-cell- and natural killer-cell-mediated cytolysis. Defects in this gene cause familial hemophagocytic lymphohistiocytosis type 2 (HPLH2), a rare and lethal autosomal recessive disorder of early childhood. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Jul 2008].
AttentionThis product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

 

FOR RESEARCH USE ONLY. Not for use in diagnostic or therapeutic procedures.

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  • Price: USD, per unit (50ul / 100ul / 200ul)

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