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Rabbit anti-Human SLC25A6 Polyclonal Antibody

The antibody against SLC25A6 was raised in Rabbit using a synthetic peptide corresponding to a sequence within amino acids 100-200 of human SLC25A6 (NP_001627.2) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IF/ICC, ELISA.

ADA-04103A

The antibody against SLC25A6 was raised in Rabbit using a synthetic peptide corresponding to a sequence within amino acids 100-200 of human SLC25A6 (NP_001627.2) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IF/ICC, ELISA.

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Specifications


Cat.No ADA-04103A ClonalityPolyclonal
Host SpeciesRabbitTarget NameSLC25A6
Target SynonymsANT; AAC3; ANT3; ANT 2; ANT 3; ANT3Y; SLC25A6FormLiquid
Species ReactivityHuman, Mouse, RatIsotypeIgG
Storage Buffer50% Glycerol, PBS with 0.05% proclin300, pH7.3.Purification MethodAffinity purification
Positive Samples293T, HT-29, K-562, Mouse thymusApplicationELISA, WB, IF/ICC

Immunogen Information


Immunogen DescriptionA synthetic peptide corresponding to a sequence within amino acids 100-200 of human SLC25A6 (NP_001627.2).Target SpeciesHuman
Immunogen SequenceLGGVDKHTQFWRYFAGNLASGGAAGATSLCFVYPLDFARTRLAADVGKSGTEREFRGLGDCLVKITKSDGIRGLYQGFSVSVQGIIIYRAAYFGVYDTAKGUniprot IDP12236
Background Information
  • Uniprot Id

    P12236

  • Target Species

    Human

  • Target Name

    SLC25A6

  • Target Full Name

    ADP/ATP translocase 3

  • Target Function

    ADP:ATP antiporter that mediates import of ADP into the mitochondrial matrix for ATP synthesis, and export of ATP out to fuel the cell. Cycles between the cytoplasmic-open state (c-state) and the matrix-open state (m-state): operates by the alternating access mechanism with a single substrate-binding site intermittently exposed to either the cytosolic (c-state) or matrix (m-state) side of the inner mitochondrial membrane. In addition to its ADP:ATP antiporter activity, also involved in mitochondrial uncoupling and mitochondrial permeability transition pore (mPTP) activity. Plays a role in mitochondrial uncoupling by acting as a proton transporter: proton transport uncouples the proton flows via the electron transport chain and ATP synthase to reduce the efficiency of ATP production and cause mitochondrial thermogenesis. Proton transporter activity is inhibited by ADP:ATP antiporter activity, suggesting that SLC25A6/ANT3 acts as a master regulator of mitochondrial energy output by maintaining a delicate balance between ATP production (ADP:ATP antiporter activity) and thermogenesis (proton transporter activity). Proton transporter activity requires free fatty acids as cofactor, but does not transport it. Also plays a key role in mPTP opening, a non-specific pore that enables free passage of the mitochondrial membranes to solutes of up to 1.5 kDa, and which contributes to cell death. It is however unclear if SLC25A6/ANT3 constitutes a pore-forming component of mPTP or regulates it.

  • Target Subcellular Location

    Mitochondrion inner membrane; Multi-pass membrane protein. Membrane; Multi-pass membrane protein.

  • Target Protein Families

    Mitochondrial carrier (TC 2.A.29) family

  • Target Tissue Specificity

    Expressed in erythrocytes (at protein level).

  • Target Research Area

    Cell Biology

  • Target Synonyms

    SLC25A6; AAC3; ANT3; CDABP0051; ADP/ATP translocase 3; ADP,ATP carrier protein 3; ADP,ATP carrier protein, isoform T2; ANT 2; Adenine nucleotide translocator 3; ANT 3; Solute carrier family 25 member 6

  • Target Background

    This gene is a member of the mitochondrial carrier subfamily of solute carrier protein genes. The product of this gene functions as a gated pore that translocates ADP from the cytoplasm into the mitochondrial matrix and ATP from the mitochondrial matrix into the cytoplasm. The protein is implicated in the function of the permability transition pore complex (PTPC), which regulates the release of mitochondrial products that induce apoptosis. The human genome contains several non-transcribed pseudogenes of this gene.

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