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Rabbit anti-Human GLUT1/SLC2A1 Polyclonal Antibody

The antibody against GLUT1/SLC2A1 was raised in Rabbit using a synthetic peptide corresponding to a sequence within amino acids 1-400 of human GLUT1/SLC2A1 (NP_006507.2) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.

ADA-10946A

The antibody against GLUT1/SLC2A1 was raised in Rabbit using a synthetic peptide corresponding to a sequence within amino acids 1-400 of human GLUT1/SLC2A1 (NP_006507.2) 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-10946A ClonalityPolyclonal
Host SpeciesRabbitTarget NameGLUT1/SLC2A1
Target SynonymsCSE; PED; DYT9; GLUT; DYT17; DYT18; EIG12; GLUT1; HTLVR; GLUT-1; SDCHCN; GLUT1DS; GLUT1/SLC2A1FormLiquid
Species ReactivityHumanIsotypeIgG
Storage Buffer50% Glycerol, PBS with 0.01% thimerosal, pH7.3.Purification MethodAffinity purification
Positive SamplesHepG2ApplicationELISA, WB

Immunogen Information


Immunogen DescriptionA synthetic peptide corresponding to a sequence within amino acids 1-400 of human GLUT1/SLC2A1 (NP_006507.2).Target SpeciesHuman
Uniprot IDP11166Immunogen Sequence
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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