Perforin 1 antibody (AA 451-500)
Quick Overview for Perforin 1 antibody (AA 451-500) (ABIN7226902)
Target
See all Perforin 1 (PRF1) AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- AA 451-500
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Purpose
- Perforin 1 Polyclonal Antibody
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Specificity
- Perforin 1 Polyclonal Antibody detects endogenous levels of Perforin 1.
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Purification
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen
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Immunogen
- Synthesized peptide derived from Perforin 1 at AA range: 451-500
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Isotype
- IgG
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Application Notes
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:10000-1:20000).
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Comment
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Primary Antibody
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 mg/mL
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Buffer
- PBS containing 50 % Glycerol, 0.5 % BSA and 0.02 % Sodium Azide.
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Preservative
- Sodium azide
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Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Storage
- -20 °C
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Storage Comment
- Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
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- Perforin 1 (PRF1) (Perforin 1 (Pore Forming Protein) (PRF1))
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Alternative Name
- Perforin 1
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Background
- Rabbit Anti-Perforin 1 Polyclonal Antibody,Perforin-1, P1, Cytolysin, Lymphocyte pore-forming protein, PFP,The protein encoded by PRF1 (perforin 1) 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 PRF1 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.,Perforin 1
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Molecular Weight
- observerd band 61kDa
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Gene ID
- 5551
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UniProt
- P14222
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Pathways
- Apoptosis, Caspase Cascade in Apoptosis
Target
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