Mouse Monoclonal Antibody Sigma Alderich A2980

Monoclonal Anti-human IgG antibody.
TMI031-0.25MG 0.25mg
EUR 169
Description: Specific to human IgG, no cross reaction with IgA, IgE, and IgM. This antibody can be paired with TMI032.

Human IgG antibody Laboratories manufactures the mouse monoclonal antibody sigma alderich a2980 reagents distributed by Genprice. The Mouse Monoclonal Antibody Sigma Alderich A2980 reagent is RUO (Research Use Only) to test human serum or cell culture lab samples. To purchase these products, for the MSDS, Data Sheet, protocol, storage conditions/temperature or for the concentration, please contact mouse monoclonal. Other Mouse products are available in stock. Specificity: Mouse Category: Monoclonal Group: Antibody Sigma

Immunoglobulin G (IgG) Monoclonal Antibody (Human)
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  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
Description: A Mouse monoclonal antibody against Human Immunoglobulin G (IgG)

Mouse Monoclonal Antibody to human IgG
50ug
EUR 270

Anti-Human IgG Rabbit Monoclonal Antibody
0.1mL
EUR 450

Anti-Human IgG Rabbit Monoclonal Antibody
5x0.1mL
EUR 1870

Monoclonal Antibody to Human IgG Fc
1mg
EUR 290

Human IgG Monoclonal Antibody [B33/20]
0.02mg
EUR 335

Human IgG Monoclonal Antibody [B33/20]
0.05mg
EUR 435

Antibody Sigma information

TTR Mouse Monoclonal Antibody (5A11)
ABM40349-003ml 0.03ml
EUR 189.6
Description: A monoclonal antibody for detection of TTR from Human. This TTR antibody is for WB, IHC-P. It is affinity-purified from mouse ascites by affinity-chromatography using the specific immunogenand is unconjugated. The antibody is produced in mouse by using as an immunogen recombinant protein of TTR

TTR Mouse Monoclonal Antibody (5A11)
ABM40349-01ml 0.1ml
EUR 346.8
Description: A monoclonal antibody for detection of TTR from Human. This TTR antibody is for WB, IHC-P. It is affinity-purified from mouse ascites by affinity-chromatography using the specific immunogenand is unconjugated. The antibody is produced in mouse by using as an immunogen recombinant protein of TTR

TTR Mouse Monoclonal Antibody (5A11)
ABM40349-02ml 0.2ml
EUR 496.8
Description: A monoclonal antibody for detection of TTR from Human. This TTR antibody is for WB, IHC-P. It is affinity-purified from mouse ascites by affinity-chromatography using the specific immunogenand is unconjugated. The antibody is produced in mouse by using as an immunogen recombinant protein of TTR

TTR (5A11) Mouse Monoclonal Antibody
EM1356-100ul 100ul
EUR 124
Description: A Mouse Monoclonal antibody against TTR (5A11) from Human. This antibody is tested and validated for WB, ELISA, IHC

TTR (5A11) Mouse Monoclonal Antibody
EM1356-50ul 50ul
EUR 74
Description: A Mouse Monoclonal antibody against TTR (5A11) from Human. This antibody is tested and validated for WB, ELISA, IHC

TTR Mouse Monoclonal Antibody(4A12)
RA10188-100ul 100 ul
EUR 298

TTR Mouse Monoclonal Antibody(4A12)
RA10188-50ul 50 ul
EUR 198

TTR Mouse Monoclonal Antibody(5A11)
RA10192-100ul 100 ul
EUR 298

TTR Mouse Monoclonal Antibody(5A11)
RA10192-50ul 50 ul
EUR 198

P53 Mouse Monoclonal Antibody(4A12)
RA10273-100ul 100 ul
EUR 298

P53 Mouse Monoclonal Antibody(4A12)
RA10273-50ul 50 ul
EUR 198

TTR mouse Monoclonal Antibody(4A12)
BT-MCA1246-100ul 100ul Ask for price
Description: This gene encodes transthyretin, one of the three prealbumins including alpha-1-antitrypsin, transthyretin and orosomucoid. Transthyretin is a carrier protein; it transports thyroid hormones in the plasma and cerebrospinal fluid, and also transports retinol (vitamin A) in the plasma. The protein consists of a tetramer of identical subunits. More than 80 different mutations in this gene have been reported; most mutations are related to amyloid deposition, affecting predominantly peripheral nerve and/or the heart, and a small portion of the gene mutations is non-amyloidogenic. The diseases caused by mutations include amyloidotic polyneuropathy, euthyroid hyperthyroxinaemia, amyloidotic vitreous opacities, cardiomyopathy, oculoleptomeningeal amyloidosis, meningocerebrovascular amyloidosis, carpal tunnel syndrome, etc.

TTR mouse Monoclonal Antibody(4A12)
BT-MCA1246-20ul 20ul Ask for price
Description: This gene encodes transthyretin, one of the three prealbumins including alpha-1-antitrypsin, transthyretin and orosomucoid. Transthyretin is a carrier protein; it transports thyroid hormones in the plasma and cerebrospinal fluid, and also transports retinol (vitamin A) in the plasma. The protein consists of a tetramer of identical subunits. More than 80 different mutations in this gene have been reported; most mutations are related to amyloid deposition, affecting predominantly peripheral nerve and/or the heart, and a small portion of the gene mutations is non-amyloidogenic. The diseases caused by mutations include amyloidotic polyneuropathy, euthyroid hyperthyroxinaemia, amyloidotic vitreous opacities, cardiomyopathy, oculoleptomeningeal amyloidosis, meningocerebrovascular amyloidosis, carpal tunnel syndrome, etc.

TTR mouse Monoclonal Antibody(4A12)
BT-MCA1246-50ul 50ul Ask for price
Description: This gene encodes transthyretin, one of the three prealbumins including alpha-1-antitrypsin, transthyretin and orosomucoid. Transthyretin is a carrier protein; it transports thyroid hormones in the plasma and cerebrospinal fluid, and also transports retinol (vitamin A) in the plasma. The protein consists of a tetramer of identical subunits. More than 80 different mutations in this gene have been reported; most mutations are related to amyloid deposition, affecting predominantly peripheral nerve and/or the heart, and a small portion of the gene mutations is non-amyloidogenic. The diseases caused by mutations include amyloidotic polyneuropathy, euthyroid hyperthyroxinaemia, amyloidotic vitreous opacities, cardiomyopathy, oculoleptomeningeal amyloidosis, meningocerebrovascular amyloidosis, carpal tunnel syndrome, etc.

TTR mouse Monoclonal Antibody(5A11)
BT-MCA1248-100ul 100ul Ask for price
Description: This gene encodes transthyretin, one of the three prealbumins including alpha-1-antitrypsin, transthyretin and orosomucoid. Transthyretin is a carrier protein; it transports thyroid hormones in the plasma and cerebrospinal fluid, and also transports retinol (vitamin A) in the plasma. The protein consists of a tetramer of identical subunits. More than 80 different mutations in this gene have been reported; most mutations are related to amyloid deposition, affecting predominantly peripheral nerve and/or the heart, and a small portion of the gene mutations is non-amyloidogenic. The diseases caused by mutations include amyloidotic polyneuropathy, euthyroid hyperthyroxinaemia, amyloidotic vitreous opacities, cardiomyopathy, oculoleptomeningeal amyloidosis, meningocerebrovascular amyloidosis, carpal tunnel syndrome, etc.

TTR mouse Monoclonal Antibody(5A11)
BT-MCA1248-20ul 20ul Ask for price
Description: This gene encodes transthyretin, one of the three prealbumins including alpha-1-antitrypsin, transthyretin and orosomucoid. Transthyretin is a carrier protein; it transports thyroid hormones in the plasma and cerebrospinal fluid, and also transports retinol (vitamin A) in the plasma. The protein consists of a tetramer of identical subunits. More than 80 different mutations in this gene have been reported; most mutations are related to amyloid deposition, affecting predominantly peripheral nerve and/or the heart, and a small portion of the gene mutations is non-amyloidogenic. The diseases caused by mutations include amyloidotic polyneuropathy, euthyroid hyperthyroxinaemia, amyloidotic vitreous opacities, cardiomyopathy, oculoleptomeningeal amyloidosis, meningocerebrovascular amyloidosis, carpal tunnel syndrome, etc.

TTR mouse Monoclonal Antibody(5A11)
BT-MCA1248-50ul 50ul Ask for price
Description: This gene encodes transthyretin, one of the three prealbumins including alpha-1-antitrypsin, transthyretin and orosomucoid. Transthyretin is a carrier protein; it transports thyroid hormones in the plasma and cerebrospinal fluid, and also transports retinol (vitamin A) in the plasma. The protein consists of a tetramer of identical subunits. More than 80 different mutations in this gene have been reported; most mutations are related to amyloid deposition, affecting predominantly peripheral nerve and/or the heart, and a small portion of the gene mutations is non-amyloidogenic. The diseases caused by mutations include amyloidotic polyneuropathy, euthyroid hyperthyroxinaemia, amyloidotic vitreous opacities, cardiomyopathy, oculoleptomeningeal amyloidosis, meningocerebrovascular amyloidosis, carpal tunnel syndrome, etc.