DLK1 hFc Chimera, Human
DLK1 HFc Chimera, Human

The purity of DLK1 hFc Chimera, Human is greater than 95% as determined by SEC-HPLC.

DLK1 HFc Chimera, Human

DLK1 hFc Chimera, Human on Bis-Tris PAGE under reduced condition. The purity is greater than 95%.

DLK1 hFc Chimera, Human

paternally inherited genetic defects of DLK1 were identified in four families with nonsyndromic CPP and a metabolic phenotype. DLK1 encodes a transmembrane protein that is important for adipose tissue homeostasis and neurogenesis and is located in the imprinted chromosome 14q32 region associated with Temple syndrome.
Z05221
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Product Introduction
Species Human
Protein Construction
DLK1 (Ala24-Gln303)
Accession # P80370-1		 hFc
N-term C-term
Purity > 95% as determined by Bis­Tris PAGE 
> 95% as determined by HPLC
Endotoxin Level Less than 1EU per μg by the LAL method.
Expression System HEK293
Theoretical Molecular Weight 56.58 kDa
Apparent Molecular Weight Due to glycosylation, the protein migrates to 70-80 kDa based on Bis-Tris PAGE result.
Formulation Lyophilized from 0.22μm filtered solution in PBS (pH 7.4).
Reconstitution Centrifuge the tube before opening. Reconstituting to a concentration more than 100 μg/ml is recommended. Dissolve the lyophilized protein in distilled water.
Storage & Stability Upon receiving, the product remains stable up to 6 months at -20 °C or below. Upon reconstitution, the product should be stable for 3 months at -80 °C. Avoid repeated freeze-thaw cycles.

Examples
  • DLK1 HFc Chimera, Human
    • DLK1 HFc Chimera, Human

    The purity of DLK1 hFc Chimera, Human is greater than 95% as determined by SEC-HPLC.

  • DLK1 HFc Chimera, Human
    • DLK1 HFc Chimera, Human

    DLK1 hFc Chimera, Human on Bis-Tris PAGE under reduced condition. The purity is greater than 95%.


Background
Target Background paternally inherited genetic defects of DLK1 were identified in four families with nonsyndromic CPP and a metabolic phenotype. DLK1 encodes a transmembrane protein that is important for adipose tissue homeostasis and neurogenesis and is located in the imprinted chromosome 14q32 region associated with Temple syndrome.
Synonyms pG2; FA1; DLK; DLK1; DLK-1; Pref1; secredeltin; ZOG

For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use.