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FGA

Anti-FGA Products
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- Class: Class II
- Antigen: cit fibrinogen-alpha
- Antigen Species: Human
- Peptide: QDFTN[cit]INKLKNS
- Conjugate: Biotin
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- Derivation: Mouse
- Species Reactivity: Human
- Type: Mouse IgG1
- Application: WB, IHC, ELISA
- Mouse Anti-FGA Recombinant Antibody (clone 1-A7) (VS3-QX425)
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- Derivation: Mouse
- Species Reactivity: Human
- Type: Mouse IgA
- Application: WB, IHC, ELISA
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- Derivation: Mouse
- Species Reactivity: Human
- Type: Mouse IgG1
- Application: WB, IHC, ELISA
- Mouse Anti-FGA Recombinant Antibody (clone 3B6) (FAMAB-1141CQ)
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- Species Reactivity: Human
- Type: Mouse IgG3
- Application: LFA (Collodial Gold), ELISA
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- Species Reactivity: Human
- Type: Mouse antibody
- Application: ELISA
- Mouse Anti-FGA Recombinant Antibody (clone 27G2) (MOB-1770z)
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- Derivation: Mouse
- Species Reactivity: Human
- Type: Mouse IgG1, κ
- Application: WB, ELISA, IHC
- Recombinant Anti-Human FGA VHH Single Domain Antibody (NAB-962-sdAb)
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- Species Reactivity: Human
- Type: Llama VHH
- Application: IHC, IP, FC, Neut, FUNC
- Mouse Anti-FGA Recombinant Antibody (clone LJ-155B16) (EPAF-0193LC)
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- Species Reactivity: Human
- Type: Mouse IgG
- Application: Block, ELISA
- Mouse Anti-FGA Recombinant Antibody (clone LJ-134B29) (EPAF-0190LC)
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- Species Reactivity: Human
- Type: Mouse IgG
- Application: Block, ELISA
- Anti-Mouse FGA Immunohistochemistry Kit (VS-0525-XY2510)
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- Species Reactivity: Human, Mouse, Rat
- Target: FGA
- Application: IHC
- Anti-FGA Immunohistochemistry Kit (VS-0525-XY2509)
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- Species Reactivity: Human
- Target: FGA
- Application: IHC
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- Species Reactivity: Human, Mouse, Rat
- Type: Rabbit IgG
- Application: WB, IHC-P, ICC, IF, IP, FC
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- Derivation: Phage display library
- Species Reactivity: Human
- Type: Rabbit IgG
- Application: ICC, IF, IHC-P, IP, WB
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For Research Use Only. Not For Clinical Use.
This gene encodes the alpha subunit of the coagulation factor fibrinogen, which is a component of the blood clot. Following vascular injury, the encoded preproprotein is proteolytically processed by thrombin during the conversion of fibrinogen to fibrin. Mutations in this gene lead to several disorders, including dysfibrinogenemia, hypofibrinogenemia, afibrinogenemia and renal amyloidosis. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that undergoes proteolytic processing. [provided by RefSeq, Jan 2016]