IFNA7 抗体应用：WB 1:500-2000 ELISA 1:5000-20000function:Produced by macrophages, IFN-alpha have antiviral activities. Interferon stimulates the production of two enzymes: a protein kinase and an oligoadenylate synthetase.,similarity:Belongs to the alpha/beta interferon family.,

IFNA8抗体应用：WB 1:500-2000 ELISA 1:5000-20000function:Produced by macrophages, IFN-alpha have antiviral activities. Interferon stimulates the production of two enzymes: a protein kinase and an oligoadenylate synthetase.,similarity:Belongs to the alpha/beta interferon family.,

IFNK抗体应用：WB 1:500-2000 ELISA 1:5000-20000interferon kappa(IFNK) Homo sapiens This gene encodes a member of the type I interferon family. Type I interferons are a group of related glycoproteins that play an important role in host defenses against viral infections. This protein is expressed in keratinocytes and the gene is found on chromosome 9, adjacent to the type I interferon cluster. [provided by RefSeq, Jul 2008],

IFRD1抗体应用：WB 1:500-2000 ELISA 1:5000-20000interferon related developmental regulator 1(IFRD1) Homo sapiens This gene is an immediate early gene that encodes a protein related to interferon-gamma. This protein may function as a transcriptional co-activator/repressor that controls the growth and differentiation of specific cell types during embryonic development and tissue regeneration. Mutations in this gene are associated with sensory/motor neuropathy with ataxia. This gene may also be involved in modulating the pathogenesis of cystic fibrosis lung disease. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Oct 2010],

IFRD2抗体应用：WB 1:500-2000 ELISA 1:5000-20000similarity:Belongs to the IFRD family.,tissue specificity:Expressed in a variety of tissues.,

IFT1B抗体应用：WB 1:500-2000 ELISA 1:5000-20000similarity:Belongs to the IFIT family.,similarity:Contains 8 TPR repeats.,

IFT46抗体应用：WB 1:500-2000

IGF2抗体应用：WB 1:500-2000 ELISA 1:5000-20000insulin like growth factor 2(IGF2) Homo sapiens This gene encodes a member of the insulin family of polypeptide growth factors, which are involved in development and growth. It is an imprinted gene, expressed only from the paternal allele, and epigenetic changes at this locus are associated with Wilms tumour, Beckwith-Wiedemann syndrome, rhabdomyosarcoma, and Silver-Russell syndrome. A read-through INS-IGF2 gene exists, whose 5' region overlaps the INS gene and the 3' region overlaps this gene. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2010],

IGFL1抗体应用：WB 1:500-2000 ELISA 1:5000-20000IGF like family member 1(IGFL1) Homo sapiens The protein encoded by this gene is a member of the insulin-like growth factor family of signaling molecules. The encoded protein is synthesized as a precursor protein and is proteolytically cleaved to form a secreted mature peptide. The mature peptide binds to a receptor, which in mouse was found on the cell surface of T cells. Increased expression of this gene may be linked to psoriasis. [provided by RefSeq, Aug 2016],

IGFL2抗体应用：WB 1:500-2000 ELISA 1:5000-20000IGF like family member 2(IGFL2) Homo sapiens IGFL2 belongs to the insulin-like growth factor (IGF; see MIM 147440) family of signaling molecules that play critical roles in cellular energy metabolism and in growth and development, especially prenatal growth (Emtage et al., 2006 [PubMed 16890402]).[supplied by OMIM, Mar 2008],