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Rabbit anti-Human SLC2A1 Polyclonal Antibody

The antibody against SLC2A1 was raised in rabbit using the Human SLC2A1,GLUT1 as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB, IF.

ADC-51161A

The antibody against SLC2A1 was raised in rabbit using the Human SLC2A1,GLUT1 as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB, IF.

$600.00

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Specifications


Cat.No ADC-51161A ClonalityPolyclonal
Host SpeciesRabbitTarget NameSLC2A1
Target Synonymsfacilitated glucose transporter member 1 antibody, member 1 antibody; Solute carrier family 2 antibody; Solute carrier family 2FormLiquid
Species ReactivityHuman, Mouse, RatIsotypeIgG
Storage Buffer50% Glycerol, Avoid freeze / thaw cycles., PBS with 0.02% sodium azidePurification MethodAntigen affinity purified
ConjugateNon-conjugatedApplicationELISA, IF, WB
StorageUpon receipt

Immunogen Information


Immunogen DescriptionHuman SLC2A1,GLUT1Target SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDP11166
Background Information
  • Uniprot Id

    P11166

  • Target Species

    Human

  • Target Name

    SLC2A1

  • Target Full Name

    Solute carrier family 2, facilitated glucose transporter member 1

  • Target Function

    Facilitative glucose transporter, which is responsible for constitutive or basal glucose uptake. Has a very broad substrate specificity; can transport a wide range of aldoses including both pentoses and hexoses. Most important energy carrier of the brain: present at the blood-brain barrier and assures the energy-independent, facilitative transport of glucose into the brain. In association with BSG and NXNL1, promotes retinal cone survival by increasing glucose uptake into photoreceptors.

  • Target Involvement

    GLUT1 deficiency syndrome 1 (GLUT1DS1); GLUT1 deficiency syndrome 2 (GLUT1DS2); Epilepsy, idiopathic generalized 12 (EIG12); Dystonia 9 (DYT9); Stomatin-deficient cryohydrocytosis with neurologic defects (SDCHCN)

  • Target Subcellular Location

    Cell membrane; Multi-pass membrane protein. Melanosome. Photoreceptor inner segment.

  • Target Protein Families

    Major facilitator superfamily, Sugar transporter (TC 2.A.1.1) family, Glucose transporter subfamily

  • Target Tissue Specificity

    Detected in erythrocytes (at protein level). Expressed at variable levels in many human tissues.

  • Target Research Area

    Metabolism

  • Target Synonyms

    Choreoathetosis/spasticity episodic (paroxysmal choreoathetosis/spasticity); CSE; DYT17; DYT18; DYT9; EIG12; erythrocyte/brain; Erythrocyte/hepatoma glucose transporter; facilitated glucose transporter member 1; Glucose transporter 1; Glucose transporter type 1; Glucose transporter type 1, erythrocyte/brain; GLUT ; GLUT-1; GLUT1; GLUT1DS; GLUTB; GT1; GTG1; Gtg3; GTR1_HUMAN; HepG2 glucose transporter; HTLVR; Human T cell leukemia virus (I and II) receptor; MGC141895; MGC141896; PED; RATGTG1; Receptor for HTLV 1 and HTLV 2; SLC2A1; Solute carrier family 2 (facilitated glucose transporter), member 1; Solute carrier family 2; Solute carrier family 2, facilitated glucose transporter member 1

  • Target Background

    This gene encodes a major glucose transporter in the mammalian blood-brain barrier. The encoded protein is found primarily in the cell membrane and on the cell surface, where it can also function as a receptor for human T-cell leukemia virus (HTLV) I and II. Mutations in this gene have been found in a family with paroxysmal exertion-induced dyskinesia.

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