DLK1, His, Human
DLK1, His, Human

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

DLK1, His, Human

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

DLK1, His, 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.
Z05222
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Product Introduction
Species Human
Protein Construction
DLK1 (Ala24-Gln303)
Accession # P80370-1		 His
N-term C-term
Purity > 95% as determined by Bis-­Tris PAGE 
Endotoxin Level Less than 1EU per μg by the LAL method.
Biological Activity Measured by its binding ability in a functional ELISA. Test result was comparable to standard batch.
Expression System HEK293
Theoretical Molecular Weight 30.9 kDa
Apparent Molecular Weight Due to glycosylation, the protein migrates to 40-50 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 for 6 months at -20℃ or below. Upon reconstitution, the product should be stable for 3 months at -80℃. Avoid repeated freeze-thaw cycles.

Examples
  • DLK1, His, Human
    • DLK1, His, Human

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

  • DLK1, His, Human
    • DLK1, His, Human

    DLK1, His, 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.