PODO抗体应用：WB 1:500-2000 ELISA 1:5000-20000NPHS2, podocin(NPHS2) Homo sapiens This gene encodes a protein that plays a role in the regulation of glomerular permeability. Mutations in this gene cause steroid-resistant nephrotic syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014],

POGZ抗体应用：WB 1:500-2000 ELISA 1:5000-20000pogo transposable element with ZNF domain(POGZ) Homo sapiens The protein encoded by this gene appears to be a zinc finger protein containing a transposase domain at the C-terminus. This protein was found to interact with the transcription factor SP1 in a yeast two-hybrid system. Alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Aug 2010],

POK17抗体应用：WB 1:500-2000

POK2抗体应用：WB 1:500-2000

POK20抗体应用：WB 1:500-2000

POK3抗体应用：WB 1:500-2000

POK5抗体应用：WB 1:500-2000

POK6抗体应用：WB 1:500-2000

POLH抗体应用：WB 1:500-2000 ELISA 1:5000-20000DNA polymerase eta(POLH) Homo sapiens This gene encodes a member of the Y family of specialized DNA polymerases. It copies undamaged DNA with a lower fidelity than other DNA-directed polymerases. However, it accurately replicates UV-damaged DNA; when thymine dimers are present, this polymerase inserts the complementary nucleotides in the newly synthesized DNA, thereby bypassing the lesion and suppressing the mutagenic effect of UV-induced DNA damage. This polymerase is thought to be involved in hypermutation during immunoglobulin class switch recombination. Mutations in this gene result in XPV, a variant type of xeroderma pigmentosum. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2014],

POLK抗体应用：WB 1:500-2000 This gene encodes a member of the DNA polymerase type-Y family of proteins. The encoded protein is a specialized DNA polymerase that catalyzes translesion DNA synthesis, which allows DNA replication in the presence of DNA lesions. Human cell lines lacking a functional copy of this gene exhibit impaired genome integrity and enhanced susceptibility to oxidative damage. Mutations in this gene that impair enzyme activity may be associated with prostate cancer in human patients. [provided by RefSeq, Sep 2016],