• Target：
• RFC2

• Fields：
• >>DNA replication;>>Nucleotide excision repair;>>Mismatch repair

• Gene Name：
• RFC2

• Protein Name：
• Replication factor C subunit 2

• Human Gene Id：
• 5982

• Human Swiss Prot No：
• P35250

• Mouse Gene Id：
• 19718

• Mouse Swiss Prot No：
• Q9WUK4

• Rat Gene Id：
• 116468

• Rat Swiss Prot No：
• Q641W4

• Immunogen：
• The antiserum was produced against synthesized peptide derived from human RFC2. AA range:131-180

• Specificity：
• RFC2 Polyclonal Antibody detects endogenous levels of RFC2 protein.

• Formulation：
• Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

• Source：
• Polyclonal, Rabbit,IgG

• Dilution：
• WB 1:500-2000;IHC 1:50-300

• Purification：
• The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

• Concentration：
• 1 mg/ml

• Storage Stability：
• -15°C to -25°C/1 year(Do not lower than -25°C)

• Other Name：
• RFC2;Replication factor C subunit 2;Activator 1 40 kDa subunit;A1 40 kDa subunit;Activator 1 subunit 2;Replication factor C 40 kDa subunit;RF-C 40 kDa subunit;RFC40

• Observed Band(KD)：
• 40kD

• Background：
• This gene encodes a member of the activator 1 small subunits family. The elongation of primed DNA templates by DNA polymerase delta and epsilon requires the action of the accessory proteins, proliferating cell nuclear antigen (PCNA) and replication factor C (RFC). Replication factor C, also called activator 1, is a protein complex consisting of five distinct subunits. This gene encodes the 40 kD subunit, which has been shown to be responsible for binding ATP and may help promote cell survival. Disruption of this gene is associated with Williams syndrome. Alternatively spliced transcript variants encoding distinct isoforms have been described. A pseudogene of this gene has been defined on chromosome 2. [provided by RefSeq, Jul 2013],

• Function：
• disease:Haploinsufficiency of RFC2 may be the cause of certain cardiovascular and musculo-skeletal abnormalities observed in Williams-Beuren syndrome (WBS), a rare developmental disorder. It is a contiguous gene deletion syndrome involving genes from chromosome band 7q11.23.,function:The elongation of primed DNA templates by DNA polymerase delta and epsilon requires the action of the accessory proteins proliferating cell nuclear antigen (PCNA) and activator 1. This subunit binds ATP.,similarity:Belongs to the activator 1 small subunits family.,subunit:Heterotetramer of subunits RFC2, RFC3, RFC4 and RFC5 that can form a complex either with RFC1 or with RAD17. The former interacts with PCNA in the presence of ATP, while the latter has ATPase activity but is not stimulated by PCNA. RFC2 also interacts with PRKAR1A; the complex may be involved in cell survival.,

• Subcellular Location：
• Nucleus .

• Expression：
• Placenta,

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