Comparison

Perforin

Item no. 18-272-197578
Manufacturer GENWAY
Amount 0.1 mg
Category
Type Antibody
Applications WB
Specific against other
ECLASS 10.1 32160702
ECLASS 11.0 32160702
UNSPSC 12352203
Alias GWB-458F50
Similar products 18-272-197578
Available
Genway ID:
GWB-458F50
Isotype:
IgG
Immunogen:
Recombinant full length protein (Rat).
Antigen Species:
Rat
Target:
Perforin
Localization:
Cytoplasmic granules
Concentration:
1 mg/ml Storage
Preservative:
0. 1% Sodium Azide; Constituents: PBS
Application Note:
WB: Use at a dilution of 1/1000. MW ~70kDNot tested in other applications. Optimal dilutions/concentrations should be determined by the end user. Cellular
Localization:
Cytoplasmic granules Perforin (pore-forming protein) is originally cloned from mouse cytotoxic T-lymphocyte(CTL) (ref 1 2). It is a 555-amino acid protein with a 21-amino acid signal peptide. Perforin is a cytolytic mediator produced by killer lymphocytes and is stored in and released by cytoplasmic granules. Perforin is involved in the killing mediated by CTL which represents an important mechanism in the immune defense against tumors and virus infections (ref 3 4).
Function:
In the presence of calcium perforin polymerizes into transmembrane tubules and is capable of lysing non-specifically a variety of target cells.
Subcellular Location:
Cytoplasmic granule membrane; Multi-pass membrane protein. Note=Cytoplasmic granules of cytolytic T-lymphocytes.
Induction:
Repressed by contact with target cells.
Disease:
Defects in PRF1 are the cause of familial hemophagocytic lymphohistiocytosis type 2 (FHL2) [MIM:603553]; also known as HPLH2. Familial hemophagocytic lymphohistiocytosis (FHL) is a genetically heterogeneous rare autosomal recessive disorder. It is characterized by immune dysregulation with hypercytokinemia and defective natural killer cell function. The clinical features of the disease include fever hepatosplenomegaly cytopenia hypertriglyceridemia hypofibrinogenemia and neurological abnormalities ranging from irritability and hypotonia to seizures cranial nerve deficits and ataxia. Hemophagocytosis is a prominent feature of the disease and a non-malignant infiltration of macrophages and activated T lymphocytes in lymph nodes spleen and other organs is also found.
Similarity:
Belongs to the complement C6/C7/C8/C9 family.
Similarity:
Contains 1 C2 domain.
Similarity:
Contains 1 EGF-like domain.
Similarity:
Contains 1 MACPF domain.

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 0.1 mg
Available: In stock
available

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