製品の概要

製品の詳細

  • 由来Recombinant
  • 由来Wheat germ
  • アミノ酸配列
    • アクセッション番号Q04446
    • 生物種Human
    • 配列MAAPMTPAARPEDYEAALNAALADVPELARLLEIDPYLKPYAVDFQRRYK QFSQILKNIGENEGGIDKFSRGYESFGVHRCADGGLYCKEWAPGAEGVFL TGDFNGWNPFSYPYKKLDYGKWELYIPPKQNKSVLVPHGSKLKVVITSKS GEILYRISPWAKYVVREGDNVNYDWIHWDPEHSYEFKHSRPKKPRSLRIY ESHVGISSHEGKVASYKHFTCNVLPRIKGLGYNCIQLMAIMEHAYYASFG YQITSFFAASSRYGSPEELQELVDTAHSMGIIVLLDVVHSHASKNSADGL NMFDGTDSCYFHSGPRGTHDLWDSRLFAYSSWEVLRFLLSNIRWWLEEYR FDGFRFDGVTSMLYHHHGVGQGFSGDYSEYFGLQVDEDALTYLMLANHLV HTLCPDSITIAEDVSGMPALCSPISQGGGGFDYRLAMAIPDKWIQLLKEF KDEDWNMGDIVYTLTNRRYLEKCIAYAESHDQALVGDKSLAFWLMDAEMY TNMSVLTPFTPVIDRGIQLHKMIRLITHGLGGEGYLNFMGNEFGHPEWLD FPRKGNNESYHYARRQFHLTDDDLLRYKFLNNFDRDMNRLEERYGWLAAP QAYVSEKHEGNKIIAFERAGLLFIFNFHPSKSYTDYRVGTALPGKFKIVL DSDAAEYGGHQRLDHSTDFFSEAFEHNGRPYSLLVYIPSRVALILQNVDL PN
    • 分子量103 kDa including tags
    • 領域1 to 702

特性

Our Abpromise guarantee covers the use of ab114840 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

  • アプリケーション

    ELISA

    SDS-PAGE

    Western blot

  • 製品の状態Liquid
  • 備考Protein concentration is above or equal to 0.05 mg/ml. This protein is best used within three months from the date of receipt.
  • Concentration information loading...

前処理および保存

  • 保存方法および安定性

    Shipped on dry ice. Upon delivery aliquot and store at -80ºC. Avoid freeze / thaw cycles.

    pH: 8.00
    Constituents: 0.3% Glutathione, 0.79% Tris HCl

関連情報

  • 別名
    • 1
    • 1,4 alpha glucan branching enzyme
    • 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
    • GBE 1
    • GBE1
    • gGlucan (1,4 alpha ), branching enzyme 1
    • GLGB_HUMAN
    • Glucan (1,4 alpha) branching enzyme
    • Glycogen branching enzyme
    • Glycogen storage disease type IV
    • Glycogen-branching enzyme
    • GSD4
    • OTTHUMP00000213788
    • OTTHUMP00000213833
    see all
  • 機能Required for sufficient glycogen accumulation. The alpha 1-6 branches of glycogen play an important role in increasing the solubility of the molecule and, consequently, in reducing the osmotic pressure within cells.
  • 組織特異性Highest levels found in liver and muscle.
  • パスウェイGlycan biosynthesis; glycogen biosynthesis.
  • 関連疾患Defects in GBE1 are the cause of glycogen storage disease type 4 (GSD4) [MIM:232500]; also known as Andersen disease. GSD4 is a metabolic disorder characterized by the accumulation of an amylopectin-like polysaccharide. The typical clinical manifestation is liver disease of childhood, progressing to lethal hepatic cirrhosis. Most children with this condition die before two years of age. However, the liver disease is not always progressive. No treatment apart from liver transplantation has been found to prevent progression of the disease. There is also a neuromuscular form of GSD4 that varies in onset (perinatal, congenital, juvenile, or adult) and severity.
    Note=Neuromuscular perinatal glycogen storage disease type 4 is associated with non-immune hydrops fetalis, a generalized edema of the fetus with fluid accumulation in the body cavities due to non-immune causes. Non-immune hydrops fetalis is not a diagnosis in itself but a symptom, a feature of many genetic disorders, and the end-stage of a wide variety of disorders.
    Defects in GBE1 are the cause of adult polyglucosan body disease (APBD) [MIM:263570]. APBD is a late-onset, slowly progressive disorder affecting the central and peripheral nervous systems. Patients typically present after age 40 years with a variable combination of cognitive impairment, pyramidal tetraparesis, peripheral neuropathy, and neurogenic bladder. Other manifestations include cerebellar dysfunction and extrapyramidal signs. The pathologic hallmark of APBD is the widespread accumulation of round, intracellular polyglucosan bodies throughout the nervous system, which are confined to neuronal and astrocytic processes.
  • 配列類似性Belongs to the glycosyl hydrolase 13 family.
  • Information by UniProt

Recombinant Human GBE1 protein 画像

  • ab114840 analysed by 12.5% SDS-PAGE and stained with Coomassie Blue.

Recombinant Human GBE1 protein (ab114840) 使用論文

ab114840 has not yet been referenced specifically in any publications.

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