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RPA32 Polyclonal Antibody, 100ul Sampling Tubes Mutations in VIM causes a

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RPA32 Polyclonal Antibody, 100ul Sampling Tubes Mutations in VIM causes aRPA2 (Replication Protein A2) is a Protein Coding gene. Diseases associated with RPA2 include xeroderma pigmentosum, group a and ataxia telangiectasia. Among its related pathways are DNA strand elongation andFanconi anemia pathway. GO annotations related to this gene include nucleic acid binding and ubiquitin protein ligase binding. An important paralog of this gene is RPA4.

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Description

Mutations in VIM causes a dominant

Capacity:5/15mL × 28

and may regulate imprinting in this region

An important paralog of this gene is MRGPRX4

is a nuclear protein involved in cell cycle progression

RPA32 Polyclonal Antibody, 100ul Sampling Tubes Mutations in VIM causes aRPA2 (Replication Protein A2) is a Protein Coding gene. Diseases associated with RPA2 include xeroderma pigmentosum, group a and ataxia telangiectasia. Among its related pathways are DNA strand elongation andFanconi anemia pathway. GO annotations related to this gene include nucleic acid binding and ubiquitin protein ligase binding. An important paralog of this gene is RPA4.

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