Item no. |
E-AB-61239-120 |
Manufacturer |
Elabscience
|
Amount |
120uL |
Category |
|
Type |
Antibody Polyclonal |
Applications |
WB |
Specific against |
Human, Mouse, Rat |
Host |
Rabbit |
Isotype |
IgG |
ECLASS 10.1 |
32160702 |
ECLASS 11.0 |
32160702 |
UNSPSC |
12352203 |
Alias |
1, 1, 4 alpha glucan branching enzyme , 1, 4-alpha-glucan branching enzyme 1, 4-alpha-glucan-branching enzyme, amylo (1, 4 to 1, 6) transglucosidase , amylo (1, 4 to 1, 6) transglycosylase , Andersen disease, APBD, Brancher enzyme, GBE 1, GBE, GBE1, gGluc |
Similar products |
GBE1, 1, GBE, 4 to 1, 6) transglucosidase, 4 to 1, 6) transglycosylase, GLGB, 4 alpha glucan branching enzyme, 4-alpha-glucan-branching enzyme, Andersen disease, Brancher enzyme, GBE 1, branching enzyme 1, Glycogen branching enzyme, Glycogen storage disease type IV, Glycogen-branching enzyme, OTTHUMP00000213788, Glucan (1, 4-alpha-glucan branching enzyme 1, amylo (1, amylo (1, APBD, gGlucan (1, 4 alpha ), 4 alpha) branching enzyme, GSD4, OTTHUMP00000213833 |
Available |
|
Research Areas |
Cancer, Metabolism, Signal Transduction |
Synonyms |
1, 1, 4 alpha glucan branching enzyme , 1, 4-alpha-glucan branching enzyme 1, 4-alpha-glucan-branching enzyme, amylo (1, 4 to 1, 6) transglucosidase , amylo (1, 4 to 1, 6) transglycosylase , Andersen disease, APBD, Brancher enzyme, GBE 1, GBE, GBE1, gGlucan (1, 4 alpha ), branching enzyme 1, GLGB, Glucan (1, 4 alpha) branching enzyme , Glycogen branching enzyme , Glycogen storage disease type IV, Glycogen-branching enzyme, GSD4, OTTHUMP00000213788, OTTHUMP00000213833 |
Swissprot |
Q04446 |
Background |
The protein encoded by this gene is a glycogen branching enzyme that catalyzes the transfer of alpha-1, 4-linked glucosyl units from the outer end of a glycogen chain to an alpha-1, 6 position on the same or a neighboring glycogen chain. Branching of the chains is essential to increase the solubility of the glycogen molecule and, consequently, in reducing the osmotic pressure within cells. Highest level of this enzyme are found in liver and muscle. Mutations in this gene are associated with glycogen storage disease IV (also known as Andersen's disease). |
Concentration |
1 mg/mL |
Storage |
Store at -20C. Avoid freeze / thaw cycles. |
Immunogen |
Recombinant protein of human GBE1 |
Buffer |
PBS with 0.02% sodium azide and 50% glycerol pH 7.4. |
Purification Method |
Affinity purification |
Dilution |
WB 1:500 - 1:2000 |
Conjugation |
Unconjugated |
Calculated MW |
80kDa |
Observed MW |
75kDa |
Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.
All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.