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GBE1 Polyclonal Antibody

GBE1 Polyclonal Antibody

ArtNr	E-AB-61239-120
Hersteller	Elabscience
Menge	120uL
Kategorie	Antibodies Western Blot Primary Antibodies
Typ	Antibody Polyclonal
Applikationen	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
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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

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Alle Produkte sind nur für Forschungszwecke bestimmt. Nicht für den menschlichen, tierärztlichen oder therapeutischen Gebrauch.

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Menge: 120uL

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Lieferung vsl. bis 06.09.2024

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