中文名稱：DLK1抗原（重組蛋白）

英文名稱：DLK1 Antigen (Recombinant Protein)

儲存：冷凍（-20℃）

相關類別：抗原

概述

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

技術規格

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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ELISA試劑盒

PCR試劑盒

生化試劑盒

農殘檢測試劑盒

細胞庫

基礎培養基

完全培養基

原代細胞

細胞專用培養基

細胞系

菌株

生化試劑

病理染色液

科研抗體

標準品

血清

形態病理檢測

分子病理

超微病理

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DLK1抗原（重組蛋白）

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.