MU-alpha-GAL |
MB1135 |
Bio Basic |
100mg |
EUR 188.41 |
|
Ige Antibody Laboratories manufactures the ige alpha gal 1 3 antibody reagents distributed by Genprice. The Ige Alpha Gal 1 3 Antibody 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 ige antibody. Other Ige products are available in stock. Specificity: Ige Category: Alpha Group: Gal 1
Beta-1, 3-Gal-T4 Polyclonal Antibody |
Abbkine |
0.2ml |
EUR 496.8 |
|
Description: A polyclonal antibody for detection of Beta-1, 3-Gal-T4 from Human. This Beta-1, 3-Gal-T4 antibody is for WB, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the Internal region of human ?-1,3-Gal-T4 at AA range: 150-230 |
Beta-1, 3-Gal-TL Polyclonal Antibody |
Abbkine |
0.03ml |
EUR 189.6 |
|
Description: A polyclonal antibody for detection of Beta-1, 3-Gal-TL from Human. This Beta-1, 3-Gal-TL antibody is for WB, IHC-P, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the C-terminal region of human ?-1,3-Gal-TL at AA range: 420-500 |
Beta-1, 3-Gal-TL Polyclonal Antibody |
Abbkine |
0.1ml |
EUR 346.8 |
|
Description: A polyclonal antibody for detection of Beta-1, 3-Gal-TL from Human. This Beta-1, 3-Gal-TL antibody is for WB, IHC-P, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the C-terminal region of human ?-1,3-Gal-TL at AA range: 420-500 |
Beta-1, 3-Gal-TL Polyclonal Antibody |
Abbkine |
0.2ml |
EUR 496.8 |
|
Description: A polyclonal antibody for detection of Beta-1, 3-Gal-TL from Human. This Beta-1, 3-Gal-TL antibody is for WB, IHC-P, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the C-terminal region of human ?-1,3-Gal-TL at AA range: 420-500 |
Beta-1, 3-Gal-T2 Polyclonal Antibody |
Abbkine |
0.03ml |
EUR 189.6 |
|
Description: A polyclonal antibody for detection of Beta-1, 3-Gal-T2 from Human, Mouse. This Beta-1, 3-Gal-T2 antibody is for IHC-P, IF, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the C-terminal region of human ?-1,3-Gal-T2 at AA range: 350-430 |
Beta-1, 3-Gal-T2 Polyclonal Antibody |
Abbkine |
0.1ml |
EUR 346.8 |
|
Description: A polyclonal antibody for detection of Beta-1, 3-Gal-T2 from Human, Mouse. This Beta-1, 3-Gal-T2 antibody is for IHC-P, IF, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the C-terminal region of human ?-1,3-Gal-T2 at AA range: 350-430 |
Beta-1, 3-Gal-T2 Polyclonal Antibody |
Abbkine |
0.2ml |
EUR 496.8 |
|
Description: A polyclonal antibody for detection of Beta-1, 3-Gal-T2 from Human, Mouse. This Beta-1, 3-Gal-T2 antibody is for IHC-P, IF, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the C-terminal region of human ?-1,3-Gal-T2 at AA range: 350-430 |
Gal 1 information
GCS alpha-1 Antibody |
DF8551 |
Affbiotech |
200ul |
EUR 420 |
Rat Interleukin-1 alpha (IL-1 alpha) Antibody |
32524-05111 |
AssayPro |
150 ug |
EUR 313.2 |
Galactosidase Alpha (GLa) Antibody |
20-abx101752 |
Abbexa |
-
EUR 477.60
-
EUR 159.60
-
EUR 1328.40
-
EUR 644.40
-
EUR 376.80
|
- 100 ug
- 10 ug
- 1 mg
- 200 ug
- 50 ug
|
|
Galactosidase Alpha (GLa) Antibody |
20-abx101753 |
Abbexa |
-
EUR 477.60
-
EUR 159.60
-
EUR 1328.40
-
EUR 644.40
-
EUR 376.80
|
- 100 ug
- 10 ug
- 1 mg
- 200 ug
- 50 ug
|
|
Galactosidase Alpha (GLA) Antibody |
20-abx112658 |
Abbexa |
|
|
|
Galactosidase Alpha (GLA) Antibody |
abx032961-400ul |
Abbexa |
400 ul |
EUR 627.6 |
|
Galactosidase Alpha (GLA) Antibody |
abx032961-80l |
Abbexa |
80 µl |
EUR 343.2 |
|
Galactosidase Alpha (GLa) Antibody |
20-abx101754 |
Abbexa |
-
EUR 477.60
-
EUR 159.60
-
EUR 1328.40
-
EUR 644.40
-
EUR 376.80
|
- 100 ug
- 10 ug
- 1 mg
- 200 ug
- 50 ug
|
|
Galactosidase Alpha (GLa) Antibody |
20-abx101755 |
Abbexa |
-
EUR 376.80
-
EUR 944.40
-
EUR 493.20
-
EUR 184.80
-
EUR 309.60
|
- 100 ug
- 1 mg
- 200 ug
- 20 ug
- 50 ug
|
|
Galactosidase Alpha (GLa) Antibody |
20-abx129508 |
Abbexa |
-
EUR 493.20
-
EUR 159.60
-
EUR 1362.00
-
EUR 661.20
-
EUR 376.80
|
- 100 ug
- 10 ug
- 1 mg
- 200 ug
- 50 ug
|
|
Galactosidase Alpha (GLa) Antibody |
20-abx131880 |
Abbexa |
-
EUR 376.80
-
EUR 944.40
-
EUR 493.20
-
EUR 184.80
-
EUR 309.60
|
- 100 ug
- 1 mg
- 200 ug
- 20 ug
- 50 ug
|
|
Galactosidase Alpha (GLA) Antibody |
20-abx001425 |
Abbexa |
-
EUR 493.20
-
EUR 710.40
-
EUR 218.40
-
EUR 376.80
|
- 100 ul
- 200 ul
- 20 ul
- 50 ul
|
|
Galactosidase Alpha (GLA) Antibody |
abx145806-100ug |
Abbexa |
100 ug |
EUR 469.2 |
|
Galactosidase alpha Antibody / Gla |
F54879-0.08ML |
NSJ Bioreagents |
0.08 ml |
EUR 140.25 |
Description: GLA is a homodimeric glycoprotein that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. This enzyme predominantly hydrolyzes ceramide trihexoside, and it can catalyze the hydrolysis of melibiose into galactose and glucose. A variety of mutations in this gene affect the synthesis, processing, and stability of this enzyme, which causes Fabry disease, a rare lysosomal storage disorder that results from a failure to catabolize alpha-D-galactosyl glycolipid moieties. |
Galactosidase alpha Antibody / Gla |
F54879-0.4ML |
NSJ Bioreagents |
0.4 ml |
EUR 322.15 |
Description: GLA is a homodimeric glycoprotein that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. This enzyme predominantly hydrolyzes ceramide trihexoside, and it can catalyze the hydrolysis of melibiose into galactose and glucose. A variety of mutations in this gene affect the synthesis, processing, and stability of this enzyme, which causes Fabry disease, a rare lysosomal storage disorder that results from a failure to catabolize alpha-D-galactosyl glycolipid moieties. |
Gla Antibody / Galactosidase alpha |
R32602 |
NSJ Bioreagents |
100 ug |
EUR 356.15 |
Description: Alpha-galactosidase is a glycoside hydrolase enzyme that encoded by the GLA gene. This gene is a homodimeric glycoprotein that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. This enzyme predominantly hydrolyzes ceramide trihexoside, and it can catalyze the hydrolysis of melibiose into galactose and glucose. A variety of mutations in this gene affect the synthesis, processing, and stability of this enzyme, which causes Fabry disease, a rare lysosomal storage disorder that results from a failure to catabolize alpha-D-galactosyl glycolipid moieties. |
Gla Antibody / Galactosidase alpha |
RQ5728 |
NSJ Bioreagents |
100 ug |
EUR 356.15 |
Description: Alpha-galactosidase is a glycoside hydrolase enzyme that encoded by the GLA gene. This gene is a homodimeric glycoprotein that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. This enzyme predominantly hydrolyzes ceramide trihexoside, and it can catalyze the hydrolysis of melibiose into galactose and glucose. A variety of mutations in this gene affect the synthesis, processing, and stability of this enzyme, which causes Fabry disease, a rare lysosomal storage disorder that results from a failure to catabolize alpha-D-galactosyl glycolipid moieties. |