中文名稱：COL2A1抗原（重組蛋白）

英文名稱：COL2A1 Antigen (Recombinant Protein)

儲存：冷凍（-20℃）

相關(guān)類別：抗原

概述

Fusion protein corresponding to a region derived from 1220-1487 amino acids of human COL2A1

技術(shù)規(guī)格

Full name:

collagen, type II, alpha 1

Synonyms:

AOM, ANFH, SEDC, COL11A3

Swissprot:

P02458

Gene Accession:

BC007252

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 the alpha-1 chain of type II collagen, a fibrillar collagen found in cartilage and the vitreous humor of the eye. Mutations in this gene are associated with achondrogenesis, chondrodysplasia, early onset familial osteoarthritis, SED congenita, Langer-Saldino achondrogenesis, Kniest dysplasia, Stickler syndrome type I, and spondyloepimetaphyseal dysplasia Strudwick type. In addition, defects in processing chondrocalcin, a calcium binding protein that is the C-propeptide of this collagen molecule, are also associated with chondrodysplasia. There are two transcripts identified for this gene.

展開全部

COL2A1抗原（重組蛋白）說明書
下載

6080yyy午夜理论av片,黄片aaawww,国产色婷婷激情片,久久午夜国产精品,久久色av网址导航,销魂美女做爰免费视频,日韩黄色三级电影在线观看,在线电影人妻在线观看,日本高清成人片www网站免费,长途公共汽车上的轮杆

021-54845833/15800441009

ELISA試劑盒

PCR試劑盒

生化試劑盒

農(nóng)殘檢測試劑盒

細胞庫

基礎(chǔ)培養(yǎng)基

完全培養(yǎng)基

原代細胞

細胞專用培養(yǎng)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(tài)病理檢測

分子病理

超微病理

產(chǎn)品中心

最新產(chǎn)品

相關(guān)文章

COL2A1抗原（重組蛋白）

Full name:	collagen, type II, alpha 1
Synonyms:	AOM, ANFH, SEDC, COL11A3
Swissprot:	P02458
Gene Accession:	BC007252
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 the alpha-1 chain of type II collagen, a fibrillar collagen found in cartilage and the vitreous humor of the eye. Mutations in this gene are associated with achondrogenesis, chondrodysplasia, early onset familial osteoarthritis, SED congenita, Langer-Saldino achondrogenesis, Kniest dysplasia, Stickler syndrome type I, and spondyloepimetaphyseal dysplasia Strudwick type. In addition, defects in processing chondrocalcin, a calcium binding protein that is the C-propeptide of this collagen molecule, are also associated with chondrodysplasia. There are two transcripts identified for this gene.