IMPCT抗体应用：WB 1:500-2000

IN35抗体应用：WB 1:500-2000 ELISA 1:5000-20000function:Not yet known.,induction:By interferon gamma.,similarity:Belongs to the NMI family.,subcellular location:Nuclear following IFN treatment.,subunit:Homodimer. Also interacts with B-ATF.,tissue specificity:In a wide range of cell types, including fibroblasts, macrophages, and epithelial cells.,

INCA1抗体应用：WB 1:500-2000

INCE抗体应用：WB 1:500-2000 ELISA 1:5000-20000inner centromere protein(INCENP) Homo sapiens In mammalian cells, 2 broad groups of centromere-interacting proteins have been described: constitutively binding centromere proteins and 'passenger,' or transiently interacting, proteins (reviewed by Choo, 1997). The constitutive proteins include CENPA (centromere protein A; MIM 117139), CENPB (MIM 117140), CENPC1 (MIM 117141), and CENPD (MIM 117142). The term 'passenger proteins' encompasses a broad collection of proteins that localize to the centromere during specific stages of the cell cycle (Earnshaw and Mackay, 1994 [PubMed 8088460]). These include CENPE (MIM 117143); MCAK (MIM 604538); KID (MIM 603213); cytoplasmic dynein (e.g., MIM 600112); CliPs (e.g., MIM 179838); and CENPF/mitosin (MIM 600236). The inner centromere proteins (INCENPs) (Earnshaw and Cooke, 1991 [PubMed 1860899]), the initial members of the passenger protein group, display a broad localization alo

ING1抗体应用：WB 1:500-2000 ELISA 1:5000-20000inhibitor of growth family member 1(ING1) Homo sapiens This gene encodes a tumor suppressor protein that can induce cell growth arrest and apoptosis. The encoded protein is a nuclear protein that physically interacts with the tumor suppressor protein TP53 and is a component of the p53 signaling pathway. Reduced expression and rearrangement of this gene have been detected in various cancers. Multiple alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008],

ING2抗体应用：WB 1:500-2000 ELISA 1:5000-20000inhibitor of growth family member 2(ING2) Homo sapiens This gene is a member of the inhibitor of growth (ING) family. Members of the ING family associate with and modulate the activity of histone acetyltransferase (HAT) and histone deacetylase (HDAC) complexes and function in DNA repair and apoptosis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014],

ING3抗体应用：WB 1:500-2000 ELISA 1:5000-20000inhibitor of growth family member 3(ING3) Homo sapiens The protein encoded by this gene is similar to ING1, a tumor suppressor protein that can interact with TP53, inhibit cell growth, and induce apoptosis. This protein contains a PHD-finger, which is a common motif in proteins involved in chromatin remodeling. This gene can activate p53 trans-activated promoters, including promoters of p21/waf1 and bax. Overexpression of this gene has been shown to inhibit cell growth and induce apoptosis. Allelic loss and reduced expression of this gene were detected in head and neck cancers. Two alternatively spliced transcript variants encoding different isoforms have been observed. [provided by RefSeq, Jul 2008],

ING5抗体应用：WB 1:500-2000 ELISA 1:5000-20000inhibitor of growth family member 5(ING5) Homo sapiens This gene encodes a tumor suppressor protein that inhibits cell growth and induces apoptosis. This protein contains a PHD-type zinc finger. It interacts with tumor suppressor p53 and p300, a component of the histone acetyl transferase complex, suggesting a role in transcriptional regulation. Alternative splicing and the use of multiple promoters and 3' terminal exons results in multiple transcript variants. [provided by RefSeq, Aug 2016],

INGR2抗体应用：WB 1:500-2000 ELISA 1:5000-20000interferon gamma receptor 2 (interferon gamma transducer 1)(IFNGR2) Homo sapiens This gene (IFNGR2) encodes the non-ligand-binding beta chain of the gamma interferon receptor. Human interferon-gamma receptor is a heterodimer of IFNGR1 and IFNGR2. Defects in IFNGR2 are a cause of mendelian susceptibility to mycobacterial disease (MSMD), also known as familial disseminated atypical mycobacterial infection. MSMD is a genetically heterogeneous disease with autosomal recessive, autosomal dominant or X-linked inheritance. [provided by RefSeq, Jul 2008],

INP5E抗体应用：WB 1:500-2000 ELISA 1:5000-20000