FAM111A Rabbit pAb
Cat No.: APA3382
Size:
Product Name: | FAM111A Rabbit pAb |
Cat No.: | APA3382 |
source: | Rabbit |
reactivity: | Human |
applications: | WB,IHC,ICC/IF |
clonality: | Polyclonal |
recommended dilution: | WB: 1:1000-1:5000 IHC: 1:20 ICC/IF: 1:20 |
format: | Liquid |
isotype: | IgG |
immunogen: | Recombinant protein of human FAM111A |
calculated molecular weight: | 70 kDa |
observed molecular weight: | 70 kDa |
genbank accession number: | Q96PZ2 |
gene id (ncbi): | 63901 |
purification method: | Affinity Purification |
conjugate: | Un-conjugated |
storage: | Store at -20°C. Supplied in 50nM Tris-Glycine(pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide and 0.05% BSA. Stable for 12 months from date of receipt. |
synonyms: | KCS2; GCLEB |
category: | Primary Ab |
concentration: | 0.5mg/ml |
background: | The protein encoded by this gene is cell-cycle regulated, and has nuclear localization. The C-terminal half of the protein shares homology with trypsin-like peptidases and it contains a PCNA-interacting peptide (PIP) box, that is necessary for its co-localization with proliferating cell nuclear antigen (PCNA). Reduced expression of this gene resulted in DNA replication defects, consistent with the demonstrated role for this gene in Simian Virus 40 (SV40) viral replication. Mutations in this gene have been associated with Kenny-Caffey syndrome (KCS) type 2 and the more severe osteocraniostenosis (OCS, also known as Gracile Bone Dysplasia), both characterized by short stature, hypoparathyroidism, bone development abnormalities, and hypocalcemia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2015] |