Boster Immunoleader

ELISA/assay

Human LIFR PicoKine ELISA Kit

EK1200

1 x96 well plate

369 USD

Human LIFR PicoKine ELISA Kit

EK1200

369 USD

Sandwich ELISA kit for Quantitative Detection of Human LIFR

NSO, Q45-S833

1 x96 well plate

156pg/ml-10,000pg/ml

<10pg/ml

Sample 1: n=16; Mean(pg/ml): 1147; Standard deviation: 65.4; CV(%): 5.7 Sample 2: n=16; Mean(pg/ml): 3628; Standard deviation: 152.4; CV(%): 4.2 Sample 3: n=16; Mean(pg/ml): 6357; Standard deviation: 419.6; CV(%): 6.6

Sample 1: n=24; Mean(pg/ml): 1458; Standard deviation: 97.7; CV(%): 6.7 Sample 2: n=24; Mean(pg/ml): 3817; Standard deviation: 221.4; CV(%): 5.8 Sample 3: n=24; Mean(pg/ml): 6682; Standard deviation: 487.8; CV(%): 7.3

There is no detectable cross-reactivity with other relevant proteins.

Store at 4˚C for 6 months, at -20˚C for 12 months. Avoid multiple freeze-thaw cycles(Shipped with wet ice.)

This kit is used for quantitative detection of human LIFR in cell culture supernates, serum and plasma(heparin, EDTA).

Human

Catalog number Description Quantity - 96-well plate precoated with anti- human LIFR antibody 1 ST0000-10 Lyophilized recombinant human LIFR standard 10ng/tubex2 AR1107 Biotinylated anti- human LIFR antibody 130ul(dilution 1:100) AR1103 Avidin-Biotin-Peroxidase Complex(ABC) 130ul(dilution 1:100) AR1106-1 Sample diluent buffer 30 ml AR1106-2 Antibody diluent buffer 12ml AR1106-3 ABC diluent buffer 12ml AR1104 TMB color developing agent 10ml AR1105 TMB stop solution 10ml

LIFR, also known as CD118(Cluster of Differentiation 118), is a subunit of a receptor for leukemia inhibitory factor. This gene encodes a protein that belongs to the type I cytokine receptor family. It is mapped to 5p31.1. The LIF receptor(LIFR) is the low-affinity binding chain that, together with the high-affinity converter subunit gp130, forms a high-affinity receptor complex that mediates the action of the leukemia-inhibitory factor. LIF is a polyfunctional cytokine that affects the differentiation, survival, and proliferation of a wide variety of cells in the adult and the embryo. Mutations in this gene cause Schwartz-Jampel syndrome type 2, a disease belonging to the group of the bent-bone dysplasias. A translocation that involves the promoter of this gene, togerther with the pleiomorphic adenoma gene 1, is associated with salivary gland pleiomorphic adenoma, a common type of benign epithelial tumor of the salivary gland.

LIFR

Leukemia inhibitory factor receptor

leukemia inhibitory factor receptor alpha

CD118 CD118 antigen FLJ98106 FLJ99923 Leukemia inhibitory factor receptor alpha Leukemia inhibitory factor receptor LIF R LIF receptor LIF-R Lifr LIFR_HUMAN SJS2 STWS SWS

P42702