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Rabbit anti-Human NKX2-5 Polyclonal Antibody

The antibody against NKX2-5 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 24-137 of human NKX2-5 (NP_004378.1) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.

ADA-07940A

The antibody against NKX2-5 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 24-137 of human NKX2-5 (NP_004378.1) 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-07940A ClonalityPolyclonal
Host SpeciesRabbitTarget Namenkx2.5
Target SynonymsCSX; CSX1; VSD3; CHNG5; HLHS2; NKX2E; NKX2.5; NKX4-1; NKX2-5FormLiquid
Species ReactivityMouse, RatIsotypeIgG
Storage Buffer50% Glycerol, PBS with 0.05% proclin300, pH7.3.Purification MethodAffinity purification
Positive SamplesMouse heart, Rat heartApplicationELISA, WB

Immunogen Information


Immunogen DescriptionRecombinant fusion protein containing a sequence corresponding to amino acids 24-137 of human NKX2-5 (NP_004378.1).Target SpeciesHuman
Immunogen SequenceQRSLAAAGELSARLEATLAPSSCMLAAFKPEAYAGPEAAAPGLPELRAELGRAPSPAKCASAFPAAPAFYPRAYSDPDPAKDPRAEKKELCALQKAVELEKTEADNAERPRARRUniprot IDP52952
Background Information
  • Uniprot Id

    P52952

  • Target Species

    Human

  • Target Name

    NKX2-5

  • Target Full Name

    Homeobox protein Nkx-2.5

  • Target Function

    Transcription factor required for the development of the heart and the spleen. During heart development, acts as a transcriptional activator of NPPA/ANF in cooperation with GATA4. May cooperate with TBX2 to negatively modulate expression of NPPA/ANF in the atrioventricular canal. Binds to the core DNA motif of NPPA promoter. Together with PBX1, required for spleen development through a mechanism that involves CDKN2B repression.

  • Target Involvement

    Atrial septal defect 7, with or without atrioventricular conduction defects (ASD7); Tetralogy of Fallot (TOF); Conotruncal heart malformations (CTHM); Hypothyroidism, congenital, non-goitrous, 5 (CHNG5); Ventricular septal defect 3 (VSD3); Hypoplastic left heart syndrome 2 (HLHS2)

  • Target Subcellular Location

    Nucleus.

  • Target Protein Families

    NK-2 homeobox family

  • Target Tissue Specificity

    Expressed only in the heart.

  • Target Synonyms

    NKX2.5; mouse; homolog of; Cardiac-specific homeobox 1; Cardiac-specific homeobox; CHNG5; CSX; CSX1; FLJ52202; FLJ97166; FLJ97195; FLJ97197; FLJ99536; HLHS2; Homeobox protein CSX; Homeobox protein NK-2 homolog E; Homeobox protein Nkx 2.5; Homeobox protein Nkx-2.5; NK2 homeobox 5; NK2 transcription factor related locus 5; NK2 transcription factor related; locus 5 (Drosophila); NK2; Drosophila; homolog of; E; NKX2-5; NKX2.5; NKX25_HUMAN; Nkx2E; NKX4-1; Tinman paralog; VSD3

  • Target Background

    This gene encodes a homeobox-containing transcription factor. This transcription factor functions in heart formation and development. Mutations in this gene cause atrial septal defect with atrioventricular conduction defect, and also tetralogy of Fallot, which are both heart malformation diseases. Mutations in this gene can also cause congenital hypothyroidism non-goitrous type 5, a non-autoimmune condition. Alternative splicing results in multiple transcript variants.

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