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Home All anti-FGA antibodies

Anti-FGA Antibody EPR2919

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Specifications Related Products Conjugation/Bulk FAQs
SKU Description Amount Price Availability*  
TA307697
  • Rabbit monoclonal antibody against Fibrinogen alpha chain (clone EPR2919 )
100ul $325 3-7 Days
TA802519S
  • Purified GAPDH mouse monoclonal antibody (Loading control), clone 2D9
30ul
$100
$50*
In Stock
Add to Shopping Cart
* Buy one primary antibody, get 50% off a GAPDH loading control antibody.
WB(1)
IHC(1)

OriGene Data

ImmunogenA synthetic peptide corresponding to residues in human Fibrinogen (alpha chain) was used as an immunogen.
Clone NameEPR2919 IsotypeRabbit IgG
Species ReactivityHuman, Rat Concentration
Guaranteed Application *WB, IHC Suggested DilutionsICC: 1:50 - 100, IHC: 1:50 - 100, IP: 1:50, WB: 1:2,000 - 10,000,
BufferStore at -20C. Buffer: 50 mM Tris-Glycine (pH 7.4), 0.15 M NaCl, 40% Glycerol, 0.01% sodium azide and 0.05% BSA. Stable for 12 months from date of receipt.

Reference Data

Target NameHomo sapiens fibrinogen alpha chain (FGA), transcript variant alpha-E
Alternative NameFib2
Database LinkNP_000499
FunctionFibrinogen is a plasma glycoprotein synthesized primarily in the liver (1). It is comprised of two identical molecular halves, each consisting of three non-identical subunit polypeptides designated as A alpha, B beta- and gamma-chains held together by multiple disulfide bonds (2). Fibrinogen acts as the main factor in the formation of a blood clot by polymerization to a fibrin network and by enabling platelets to aggregate (3). The conversion of fibrinogen to fibrin is triggered by thrombin, which cleaves fibrinopeptides A and B from alpha and beta chains, and thus exposes the N-terminal polymerization sites responsible for the formation of the soft clot. The soft clot is converted into the hard clot by factor XIIIA which catalyzes the epsilon-(gamma-glutamyl)lysine cross-linking between gamma chains (stronger) and between alpha chains (weaker) of different monomers. Defects in fibrinogen are a cause of congenital afibrinogenemia, a rare autosomal recessive disorder, and amyloidosis type 8, also known as systemic non-neuropathic amyloidosis or Ostertag-type amyloidosis (4).
Related Pathway
Hemostasis

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WB Image
Western blot analysis on (A) human plasma, (B) fetal liver and (C) HepG2 cell lysates using anti-Fibrinogen alpha chain RabMAb .
IHC Image
Immunohistochemical analysis of paraffin-embedded human hepatocellular carcinoma using anti-Fibrinogen alpha chain RabMAb .

 

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