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Collagen Type lll (PT0118) mouse mAb

说明书

BYab-17959

  • 20UL ¥460 50UL ¥945 100UL ¥1350
  • 货期: 3天左右

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宿主
反应性
应用
WB;IHC;ELISA
分子量(DA)
免疫原
Synthesized peptide derived from human Collagen Type III AA range: 100-200
特异性
This antibody detects endogenous levels of human Collagen Type III. Heat-induced epitope retrieval (HIER) Citrate buffer of pH6.0/Pepsin was highly recommended as antigen repair method in paraffin se
来源
Mouse, Monoclonal/IgG1, Kappa
组成(Formulation)
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
稀释比例
IHC-p 1:200-400,WB 1:100-2000., ELISA 1:5000-20000
纯化工艺(Immunogen)
The antibody was affinity-purified from mouse ascites by affinity-chromatography using specific immunogen.
浓度
1 mg/ml
背景(Background)
collagen type III alpha 1 chain(COL3A1) Homo sapiens This gene encodes the pro-alpha1 chains of type III collagen, a fibrillar collagen that is found in extensible connective tissues such as skin, lung, uterus, intestine and the vascular system, frequently in association with type I collagen. Mutations in this gene are associated with Ehlers-Danlos syndrome types IV, and with aortic and arterial aneurysms. Two transcripts, resulting from the use of alternate polyadenylation signals, have been identified for this gene. [provided by R. Dalgleish, Feb 2008],
功能
disease:Defects in COL3A1 are a cause of Ehlers-Danlos syndrome type 3 (EDS3) [MIM:130020]; also known as benign hypermobility syndrome. EDS is a connective tissue disorder characterized by hyperextensible skin, atrophic cutaneous scars due to tissue fragility and joint hyperlaxity. EDS3 is a form of Ehlers-Danlos syndrome characterized by marked joint hyperextensibility without skeletal deformity.,disease:Defects in COL3A1 are a cause of susceptibility to aortic aneurysm abdominal (AAA) [MIM:100070]. AAA is a common multifactorial disorder characterized by permanent dilation of the abdominal aorta, usually due to degenerative changes in the aortic wall. Histologically, AAA is characterized by signs of chronic inflammation, destructive remodeling of the extracellular matrix, and depletion of vascular smooth muscle cells.,disease:Defects in COL3A1 are the cause of Ehlers-Danlos syndrome t
基因名称(Gene Name)
COL3A1
蛋白名称
Collagen alpha-1(III) chain
简称
其他名称
Fields
>>Platelet activation;>>Relaxin signaling pathway;>>AGE-RAGE signaling pathway in diabetic complications;>>Protein digestion and absorption;>>Amoebiasis;>>Diabetic cardiomyopathy
人基因ID
1281
人蛋白质序列数据库
P02461
小鼠基因ID
小鼠蛋白质序列数据库
大鼠基因ID
大鼠蛋白质序列数据库
细胞定位
Secreted, extracellular space, extracellular matrix .
组织表达
Colon carcinoma,Liver,Placenta,Skin fibroblast
储存(Storage)
-15°C to -25°C/1 year(Do not lower than -25°C)

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Collagen Type lll (PT0118) mouse mAb

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