50-113-7522
Perforin Monoclonal Antibody (dG9), Alexa Fluor™ 647, Invitrogen™
Manufacturer: Invitrogen
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | 50-113-7522-Each-of-1 | In Stock | ₹ 38,626.00 |
50-113-7522 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 38,626.00
GST (18%): ₹ 6,952.68
Total Price: ₹ 45,578.68
Antigen
Perforin
Classification
Monoclonal
Conjugate
Alexa Fluor 647
Gene
PRF1
Gene Alias
Cyta; Cytolysin; FLH2; HPLH2; lymphocyte pore forming protein; lymphocyte pore-forming protein; OMAK; OTTHUMP00000019759; P1; perforin 1; perforin 1 (pore forming protein); Perforin1; perforin-1; Pfn; PFN1; Pfp; PGFL; PIGF; PIGF-2; PLGF; pore forming protein; pore-forming protein; PRF1; Prf-1; PRF1 (pore forming protein 1); RATCYTA; RP11-710A11.3
Host Species
Mouse
Purification Method
purified
Regulatory Status
RUO
Gene ID (Entrez)
5551
Content And Storage
4° C
Form
Liquid
Applications
Flow Cytometry
Clone
dG9
Formulation
PBS with 0.1% sodium azide
Gene Accession No.
P14222
Gene Symbols
PRF1
Immunogen
Human Perforin.
Quantity
500 μL
Primary or Secondary
Primary
Target Species
Human
Product Type
Antibody
Isotype
IgG2b
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Description
- Perforin is one of the major cytolytic proteins of cytolytic granules
- Perforin is a cytolytic mediator and is stored in and released by cytoplasmic granules
- Moreover, perforin is involved in immune defense against tumors and virus infections as mediated by cytotoxic lymphocytes
- Perforin is a 555 amino acid protein with a 21 amino acid signal peptide, and has a molecular weight of 70 to 75 kD
- Perforin is a pore forming protein with a mechanism of transmembrane channel formation similar to C9, and homology between perforin and C9 have been demonstrated
- Studies show that perforin is expressed only in killer cell lines and not in helper T lymphocytes or other tumor cells tested
- Perforin is known to be a key effector molecule for T-cell- and natural killer-cell-mediated cytolysis
- Defects in the perforin 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 of perforin.