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Rabbit anti-Human APBB1 Polyclonal Antibody

The antibody against APBB1 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 359-708 of human APBB1 (NP_663722.1) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.

ADA-04451A

The antibody against APBB1 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 359-708 of human APBB1 (NP_663722.1) 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-04451A ClonalityPolyclonal
Host SpeciesRabbitTarget NameAPBB1
Target SynonymsRIR; FE65; MGC:9072; APBB1FormLiquid
Species ReactivityHuman, MouseIsotypeIgG
Storage Buffer50% Glycerol, PBS with 0.02% sodium azide, pH7.3.Purification MethodAffinity purification
Positive SamplesMouse heart, A-549, BT-474, LOVO, Mouse brain, Mouse lung, Mouse spinal cord, RajiApplicationELISA, WB

Immunogen Information


Immunogen DescriptionRecombinant fusion protein containing a sequence corresponding to amino acids 359-708 of human APBB1 (NP_663722.1).Target SpeciesHuman
Uniprot IDO00213Immunogen Sequence
Background Information
  • Uniprot Id

    O00213

  • Target Species

    Human

  • Target Name

    APBB1

  • Target Full Name

    Amyloid beta precursor protein binding family B member 1

  • Target Function

    Transcription coregulator that can have both coactivator and corepressor functions. Adapter protein that forms a transcriptionally active complex with the gamma-secretase-derived amyloid precursor protein (APP) intracellular domain. Plays a central role in the response to DNA damage by translocating to the nucleus and inducing apoptosis. May act by specifically recognizing and binding histone H2AX phosphorylated on 'Tyr-142' (H2AXY142ph) at double-strand breaks (DSBs), recruiting other pro-apoptosis factors such as MAPK8/JNK1. Required for histone H4 acetylation at double-strand breaks (DSBs). Its ability to specifically bind modified histones and chromatin modifying enzymes such as KAT5/TIP60, probably explains its transcription activation activity. Functions in association with TSHZ3, SET and HDAC factors as a transcriptional repressor, that inhibits the expression of CASP4. Associates with chromatin in a region surrounding the CASP4 transcriptional start site(s). Involved in hippocampal neurite branching and neuromuscular junction formation, as a result plays a role in spatial memory functioning. Plays a role in the maintenance of lens transparency. May play a role in muscle cell strength.

  • Target Subcellular Location

    Cell membrane. Cytoplasm. Nucleus. Cell projection, growth cone. Nucleus speckle.

  • Target Tissue Specificity

    Highly expressed in brain; strongly reduced in post-mortem elderly subjects with Alzheimer disease.

  • Target Synonyms

    Adaptor protein FE65a2; Amyloid beta (A4) precursor protein binding family B member 1; Amyloid beta A4 precursor protein binding family B; Amyloid beta A4 precursor protein binding family B member 1; Amyloid beta A4 precursor protein-binding family B member 1; Amyloid beta precursor protein binding family B member 1; APBB 1; APBB1; APBB1_HUMAN; FE 65; Fe65 protein; Protein Fe65; RIR; stat like protein

  • Target Background

    The protein encoded by this gene is a member of the Fe65 protein family. It is an adaptor protein localized in the nucleus. It interacts with the Alzheimer's disease amyloid precursor protein (APP), transcription factor CP2/LSF/LBP1 and the low-density lipoprotein receptor-related protein. APP functions as a cytosolic anchoring site that can prevent the gene product's nuclear translocation. This encoded protein could play an important role in the pathogenesis of Alzheimer's disease. It is thought to regulate transcription. Also it is observed to block cell cycle progression by downregulating thymidylate synthase expression. Multiple alternatively spliced transcript variants encoding different isoforms have been described for this gene.

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