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Rabbit anti-Human RMI2 Polyclonal Antibody

The antibody against RMI2 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 1-147 of human RMI2 (NP_689521.1) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.

ADA-01213A

The antibody against RMI2 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 1-147 of human RMI2 (NP_689521.1) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.

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Specifications


Cat.No ADA-01213A ClonalityPolyclonal
Host SpeciesRabbitTarget NameRMI2
Target SynonymsBLAP18; C16orf75; RMI2FormLiquid
Species ReactivityHumanIsotypeIgG
Storage Buffer50% Glycerol, PBS with 0.02% sodium azide, pH7.3.Purification MethodAffinity purification
Positive SamplesHeLa, MCF7ApplicationELISA, WB

Immunogen Information


Immunogen DescriptionRecombinant fusion protein containing a sequence corresponding to amino acids 1-147 of human RMI2 (NP_689521.1).Target SpeciesHuman
Immunogen SequenceMAAAADSFSGGPAGVRLPRSPPLKVLAEQLRRDAEGGPGAWRLSRAAAGRGPLDLAAVWMQGRVVMADRGEARLRDPSGDFSVRGLERVPRGRPCLVPGKYVMVMGVVQACSPEPCLQAVKMTDLSDNPIHESMWELEVEDLHRNIPUniprot IDQ96E14
Background Information
  • Uniprot Id

    Q96E14

  • Target Species

    Human

  • Target Name

    RMI2

  • Target Full Name

    RecQ-mediated genome instability protein 2

  • Target Function

    Essential component of the RMI complex, a complex that plays an important role in the processing of homologous recombination intermediates. It is required to regulate sister chromatid segregation and to limit DNA crossover. Essential for the stability, localization, and function of BLM, TOP3A, and complexes containing BLM. In the RMI complex, it is required to target BLM to chromatin and stress-induced nuclear foci and mitotic phosphorylation of BLM.

  • Target Involvement

    A homozygous deletion of RMI2 has been found in a family with a Bloom-like syndrome and is probable responsible for the phenotype. Patients manifest depigmented skin lesions, multiple cafe-au-lait macules, and growth deficiency. Cells from affected individuals show a high rate of sister chromatid exchange and increased chromosomal breaks.

  • Target Subcellular Location

    Nucleus. Note=Colocalizes with BLM at nuclear DNA repair foci.

  • Target Protein Families

    RMI2 family

  • Target Synonyms

    BLAP18; BLM-associated protein of 18 kDa; C16orf75; hRMI2; MGC24665; RecQ-mediated genome instability protein 2; RMI2; RMI2_HUMAN

  • Target Background

    RMI2 is a component of the BLM (RECQL3; MIM 604610) complex, which plays a role in homologous recombination-dependent DNA repair and is essential for genome stability (Xu et al., 2008 [PubMed 18923082]).

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