Human Interleukin 12 (IL12) CLIA Kit

The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. <br>To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.

This assay has high sensitivity and excellent specificity for detection of Interleukin 12 (IL12).<br> No significant cross-reactivity or interference between Interleukin 12 (IL12) and analogues was observed.

[interleukin 12; Interleukin-12 subunit alpha; interleukin-12 subunit alpha; interleukin 12A; Cytotoxic lymphocyte maturation factor 35 kDa subunit; CLMF p35; IL-12 subunit p35; NK cell stimulatory factor chain 1; NKSF1]