中文名称：DLK1抗原（重组蛋白）

英文名称：DLK1 Antigen (Recombinant Protein)

储存：冷冻（-20℃）

相关类别：抗原

概述

Fusion protein corresponding to C terminal 300 amino acids of human DLK1

技术规格

Full name:

delta like non-canonical Notch ligand 1

Synonyms:

DLK; FA1; ZOG; pG2; DLK-1; PREF1; Delta1; Pref-1

Swissprot:

P80370

Gene Accession:

BC007741

Purity:

>85%, as determined by Coomassie blue stained SDS-PAGE

Expression system:

Escherichia coli

Tags:

His tag C-Terminus, GST tag N-Terminus

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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DLK1抗原（重组蛋白）说明书
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细胞库

基础培养基

完全培养基

原代细胞

细胞专用培养基

细胞系

菌株

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病理染色液

科研抗体

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形态病理检测

分子病理

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DLK1抗原（重组蛋白）

Full name:	delta like non-canonical Notch ligand 1
Synonyms:	DLK; FA1; ZOG; pG2; DLK-1; PREF1; Delta1; Pref-1
Swissprot:	P80370
Gene Accession:	BC007741
Purity:	>85%, as determined by Coomassie blue stained SDS-PAGE
Expression system:	Escherichia coli
Tags:	His tag C-Terminus, GST tag N-Terminus
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.