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Recombinant Human Protein delta homolog 1 (DLK1), Truncated

This Recombinant Human Protein Delta Homolog 1 (DLK1) is a valuable addition to your neuroscience research toolbox. DLK1, also known as DLK-1 or pG2, is a transmembrane protein that plays a crucial role in the development and differentiation of various cell types, particularly in the nervous system. Studies have implicated DLK1 in numerous biological processes, including neurogenesis, adipogenesis, and cell fate determination. Our Recombinant Human DLK1 protein is produced in a mammalian cell system, ensuring proper folding and post-translational modifications. The protein consists of a partial sequence (24-303aa) and is fused with a C-terminal Flag-Myc tag for efficient purification and detection. With a purity of greater than 90% as determined by SDS-PAGE, our DLK1 protein guarantees consistent performance in your experiments. Available in both liquid and lyophilized powder forms, this high-quality protein is designed to meet the diverse demands of your neuroscience research.

ACP02792

This Recombinant Human Protein Delta Homolog 1 (DLK1) is a valuable addition to your neuroscience research toolbox. DLK1, also known as DLK-1 or pG2, is a transmembrane protein that plays a crucial role in the development and differentiation of various cell types, particularly in the nervous system. Studies have implicated DLK1 in numerous biological processes, including neurogenesis, adipogenesis, and cell fate determination.
Our Recombinant Human DLK1 protein is produced in a mammalian cell system, ensuring proper folding and post-translational modifications. The protein consists of a partial sequence (24-303aa) and is fused with a C-terminal Flag-Myc tag for efficient purification and detection. With a purity of greater than 90% as determined by SDS-PAGE, our DLK1 protein guarantees consistent performance in your experiments. Available in both liquid and lyophilized powder forms, this high-quality protein is designed to meet the diverse demands of your neuroscience research.

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Specifications


Cat.No ACP02792 Target NameDLK1
FormLiquid or Lyophilized powderExpression SystemMammalian cell
Expression Range24-303aaMol Weight32.8 kDa
Protein LengthPartialPurityGreater than 90% as determined by SDS-PAGE.
Storage Buffer5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0.

Immunogen Information


Target SpeciesHumanUniprot IDP80370
Background Information
  • Uniprot Id

    P80370

  • Target Species

    Human

  • Target Name

    DLK1

  • Target Full Name

    Protein delta homolog 1

  • Target Function

    May have a role in neuroendocrine differentiation.

  • Target Subcellular Location

    Membrane; Single-pass type I membrane protein. Cytoplasm.

  • Target Tissue Specificity

    Found within the stromal cells in close contact to the vascular structure of placental villi, yolk sac, fetal liver, adrenal cortex and pancreas and in the beta cells of the islets of Langerhans in the adult pancreas. Found also in some forms of neuroendo

  • Target Research Area

    Neuroscience

  • Target Synonyms

    Adipocyte differentiation inhibitor protein; Brevideltin; Delta like 1 homolog; Delta like homolog; Delta like protein; Delta1; DLK 1; DLK; DLK-1; DLK1; DLK1_HUMAN; FA 1; FA1; Fetal antigen 1; pG2; Preadipocyte factor 1; Pref 1; Pref; Pref1; Protein delta homolog 1; Secredeltin; ZOG

  • Target Background

    This gene encodes a transmembrane protein that contains multiple epidermal growth factor repeats that functions as a regulator of cell growth. The encoded protein is involved in the differentiation of several cell types including adipocytes. This gene is located in a region of chromosome 14 frequently showing unparental disomy, and is imprinted and expressed from the paternal allele. A single nucleotide variant in this gene is associated with child and adolescent obesity and shows polar overdominance, where heterozygotes carrying an active paternal allele express the phenotype, while mutant homozygotes are normal.

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