Cleaved-COL3A1 (G1221) rabbit pAb

Cleaved-COL3A1 (G1221) rabbit pAb

AO-06-ES1035-100

Cleaved-COL3A1 (G1221) rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES1035
Product nameCleaved-COL3A1 (G1221) rabbit pAb
ReactivityHuman;Rat;Mouse;
ApplicationsELISA
Other nameCOL3A1; Collagen alpha-1(III) chain
Size100μL
Unit price ($)248
Human gene ID1281
Human Swiss-ProtP02461
SourceRabbit
IsotypeIgG
TargetCollagen III
Fields>>Platelet activation;>>Relaxin signaling pathway;>>AGE-RAGE signaling pathway in diabetic complications;>>Protein digestion and absorption;>>Amoebiasis;>>Diabetic cardiomyopathy
Gene nameCOL3A1
Protein nameCollagen alpha-1(III) chain
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID
Mouse gene link
Mouse Swiss-ProtP08121
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID
Rat gene link
Rat Swiss-Prot
Rat Swiss link
ImmunogenThe antiserum was produced against synthesized peptide derived from human Collagen III alpha1. AA range:1172-1221
SpecificityCleaved-COL3A1 (G1221) Polyclonal Antibody detects endogenous levels of fragment of activated COL3A1 protein resulting from cleavage adjacent to G1221.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionELISA: 1/10000. Not yet tested in other applications.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)95kD
Backgroundcollagen 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],
Functiondisease: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
Subcellular locationSecreted, extracellular space, extracellular matrix .
ExpressionColon carcinoma,Liver,Placenta,Skin fibroblast,

Additional Images

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Western Blot analysis of various cells using Cleaved-COL3A1 (G1221) Polyclonal Antibody
Image 2
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Western blot analysis of lysates from A549 cells, treated with etoposide 25uM 24h, using Collagen III alpha1 (Cleaved-Gly1221) Antibody. The lane on the right is blocked with the synthesized peptide.
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: AO-06-ES1035-100
: 10 Items
Hurry! only 10 items left in stock.

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