CoraLite® Plus 488-conjugated Perforin Polyclonal antibody

Perforin Polyclonal Antibody for
Cat No. CL488-14580

产品说明书

宿主/亚型

Rabbit / IgG

种属反应性

human, mouse

应用

Perforin 1, P1, Lymphocyte pore-forming protein, HPLH2, FLH2

缓冲液配方:  PBS, Proclin 300, BSA, Glycerol
PBS, Proclin 300, BSA, Glycerol
偶联物:  CoraLite® Plus 488
规格价格库存


For other applications, we recommend the unconjugated version of this antibody, 14580-1-AP

产品信息

CL488-14580 targets Perforin in applications and shows reactivity with human, mouse samples.

经测试应用 Application Description
经测试反应性 human, mouse
免疫原

CatNo: Ag6060

Product name: Recombinant human Perforin protein

Source: e coli.-derived, PET28a

Tag: 6*His

Domain: 247-555 aa of BC063043

Sequence: EGLTDNEVEDCLTVEAQVNIGIHGSISAEAKACEEKKKKHKMTASFHQTYRERHSEVVGGHHTSINDLLFGIQAGPEQYSAWVNSLPGSPGLVDYTLEPLHVLLDSQDPRREALRRALSQYLTDRARWRDCSRPCPPGRQKSPRDPCQCVCHGSAVTTQDCCPRQRGLAQLEVTFIQAWGLWGDWFTATDAYVKLFFGGQELRTSTVWDNNNPIWSVRLDFGDVLLATGGPLRLQVWDQDSGRDDDLLGTCDQAPKSGSHEVRCNLNHGHLKFRYHARCLPHLGGGTCLDYVPQMLLGEPPGNRSGAVW

种属同源性预测
宿主/亚型 Rabbit / IgG
抗体类别 Polyclonal
产品类型 Antibody
全称 perforin 1 (pore forming protein)
别名 Perforin 1, P1, Lymphocyte pore-forming protein, HPLH2, FLH2
计算分子量 61 kDa
观测分子量 70-75 kDa
GenBank蛋白编号BC063043
基因名称 Perforin
Gene ID (NCBI) 5551
偶联类型 CoraLite® Plus 488 Fluorescent Dye
最大激发/发射波长493 nm / 522 nm
形式Liquid
纯化方式Antigen affinity purification
UNIPROT IDP14222
储存缓冲液 PBS with 50% glycerol, 0.05% Proclin300, 0.5% BSA, pH 7.3.
储存条件Store at -20°C. Avoid exposure to light. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.

背景介绍

Perforin 1 (PRF1) is one of the major cytolytic proteins of cytolytic granules. It is known to be a crucial effector molecule in cytolytic T lymphocyte and natural killer cell-mediated cytotoxicity. This protein has structural and functional similarities to complement component C9. Like C9, this protein creates transmembrane tubules and is capable of lysing nonspecifically a variety of target cells. Defects in PRF1 are the cause of familial hemophagocytic lymphohistiocytosis type 2 (FHL2), which is characterized by immune dysregulation with hypercytokinemia and defective natural killer cell function. (PMID: 2417226; 7774276; 2783486; 10583959)

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