p62 elisa kit product blog
Tags: ELISA Kit; Human ELISA Kit; p62; P62 elisa kit; Antioncogene p62 protein;
The Human p62 khdrbs1 (Catalog #MBS7221409) is an ELISA Kit and is intended for research purposes only. The product is available for immediate purchase. The MBS7221409 ELISA Kit recognizes Human p62.The p62 khdrbs1 product has the following accession number(s) (GI #189500) (NCBI Accession #AAA59990.1). Researchers may be interested in using Bioinformatics databases such as those available at The National Center for Biotechnology Information (NCBI) website for more information about accession numbers and the proteins they represent. Even researchers unfamiliar with bioinformatics databases will find the NCBI databases to be quite user friendly and useful.
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(Or you can also download the PDF Manual for complete product instructions).
Samples: Serum, plasma, Cell Culture Supernatants, body fluid and tissue homogenate
Assay Type: Sandwich
Detection Range: 2.5-50ng/mL
Sensitivity: 0.1ng/mL. Human Antioncogene p62 protein ELISA Kit or ELISA (enzyme-linked immunosorbant assays) Kits in general, are a valuable research tool for a myriad of applications in a range of scientific settings. Currently, three major types of ELISA formats are used by researchers: sandwich, competitive and indirect. Most commercially available ELISA Kits are sandwich or competitive. Commercially available ELISA Kits contain wells that have been pre-coated with the capture antibody. Please refer to the product manual for the ELISA format of your specific kit. Blood, Bone, Brain, Embryonic Tissue, Kidney, Mammary Gland, Nerve, Placenta, Prostate, Testis tissues are correlated with this protein. Adenocarcinoma, Cell Transformation, Neoplastic, Immune System Diseases, Infertility, Female, Infertility, Male, Liver Diseases, Liver Neoplasms, Lung Diseases, Nervous System Diseases, Prostatic Neoplasms are some of the diseases may be linked to Human Antioncogene p62 protein ELISA Kit. p62 also interacts with the following gene(s): FYN, GRB2, HNRNPK, KHDRBS3, LCK, PRMT1, SRC. The following patways have been known to be associated with this gene.