• Collagen Type IV mouse mAb(ABT165)
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Upingbio

YP-Ab-15654-53UL

Collagen Type IV mouse mAb(ABT165)

Collagen Type IV mouse mAb(ABT165)

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  • Reaction species: Human; Predict react with Mouse
  • Gene Name: COL4A1
  • Protein name: Collagen Type IV
  • Immunogen: Synthesized peptide derived from human Collagen Type IV
  • Specificity: The antibody can specifically recognize human Collagen Type IV protein, collagen types I, II, III and V do not respond to the anbody.
  • Composition: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.31% sodium azide.
  • Source: Mouse, Monoclonal/IgG2b, kappa
  • Dilution ratio: WB 1:1000-2000;IHC-p 1:100-500, IF 1:100-500
  • Purification process: The antibody was affinity-purified from mouse ascites by affinity-chromatography using specific immunogen.
  • Storage: -20°C/1 year
  • Other Names: Collagen alpha-1(IV) chain [Cleaved into: Arresten]
  • Background: This gene encodes a type IV collagen alpha protein. Type IV collagen proteins are integral components of basement membranes. This gene shares a bidirectional promoter with a paralogous gene on the opposite strand. The protein consists of an amino-terminal 7S domain, a triple-helix forming collagenous domain, and a carboxy-terminal non-collagenous domain. It functions as part of a heterotrimer and interacts with other extracellular matrix components such as perlecans, proteoglycans, and laminins. In addition, proteolytic cleavage of the non-collagenous carboxy-terminal domain results in a biologically active fragment known as arresten, which has anti-angiogenic and tumor suppressor properties. Mutations in this gene cause porencephaly, cerebrovascular disease, and renal and muscular defects. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014],
  • Function: disease:Defects in COL4A1 are a cause of brain small vessel disease with hemorrhage [MIM:607595]. Brain small vessel diseases underlie 20 to 30 percent of ischemic strokes and a larger proportion of intracerebral hemorrhages. Inheritance is autosomal dominant.,disease:Defects in COL4A1 are a cause of porencephaly type 1 [MIM:175780]; also known as encephaloclastic porencephaly. Porencephaly is a term used for any cavitation or cerebrospinal fluid-filled cyst in the brain. Porencephaly type 1 is usually unilateral and results from focal destructive lesions such as fetal vascular occlusion or birth trauma. Inheritance is autosomal dominant.,disease:Defects in COL4A1 are the cause of hereditary angiopathy with nephropathy, aneurysms, and muscle cramps (HANAC) [MIM:611773]. The clinical renal manifestations include hematuria and bilateral large cysts. Histologic analysis revealed complex bas
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