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GLB1 Protein (AA 24-677) (His tag)

GLB1 Origin: Human Host: Human Cells Recombinant > 95 % as determined by reducing SDS-PAGE.
Catalog No. ABIN1096122
  • Target See all GLB1 Proteins
    GLB1 (Galactosidase, beta 1 (GLB1))
    Protein Type
    Recombinant
    Protein Characteristics
    AA 24-677
    Origin
    • 9
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Human
    Source
    • 17
    • 3
    • 2
    • 2
    • 1
    • 1
    Human Cells
    Purification tag / Conjugate
    This GLB1 protein is labelled with His tag.
    Purpose
    Recombinant Human β-Galactosidase/GLB1 (C-6His)
    Sequence
    LRNATQRMFE IDYSRDSFLK DGQPFRYISG SIHYSRVPRF YWKDRLLKMK MAGLNAIQTY VPWNFHEPWP GQYQFSEDHD VEYFLRLAHE LGLLVILRPG PYICAEWEMG GLPAWLLEKE SILLRSSDPD YLAAVDKWLG VLLPKMKPLL YQNGGPVITV QVENEYGSYF ACDFDYLRFL QKRFRHHLGD DVVLFTTDGA HKTFLKCGAL QGLYTTVDFG TGSNITDAFL SQRKCEPKGP LINSEFYTGW LDHWGQPHST IKTEAVASSL YDILARGASV NLYMFIGGTN FAYWNGANSP YAAQPTSYDY DAPLSEAGDL TEKYFALRNI IQKFEKVPEG PIPPSTPKFA YGKVTLEKLK TVGAALDILC PSGPIKSLYP LTFIQVKQHY GFVLYRTTLP QDCSNPAPLS SPLNGVHDRA YVAVDGIPQG VLERNNVITL NITGKAGATL DLLVENMGRV NYGAYINDFK GLVSNLTLSS NILTDWTIFP LDTEDAVRSH LGGWGHRDSG HHDEAWAHNS SNYTLPAFYM GNFSIPSGIP DLPQDTFIQF PGWTKGQVWI NGFNLGRYWP ARGPQLTLFV PQHILMTSAP NTITVLELEW APCSSDDPEL CAVTFVDRPV IGSSVTYDHP SKPVEKRLMP PPPQKNKDSW LDHVVDHHHH HH
    Characteristics
    Recombinant Human beta-Galactosidase/GLB1 is produced with our mammalian expression system in human cells. The target protein is expressed with sequence (L24-V677) of Human GLB1 fused with a polyhistidine tag at the C-terminus.
    Purity
    > 95 % as determined by reducing SDS-PAGE.
    Sterility
    0.2 μm filtered
    Endotoxin Level
    Less than 0.1 ng/μg (1 IEU/μg) as determined by LAL test
    Top Product
    Discover our top product GLB1 Protein
  • Restrictions
    For Research Use only
  • Format
    Liquid
    Reconstitution
    It is not recommended to reconstitute to a concentration less than 100 μg/mL.
    Dissolve the lyophilized protein in ddH2O.
    Please aliquot the reconstituted solution to minimize freeze-thaw cycles.
    Buffer
    Supplied as a 0.2 μm filtered solution of 20 mM TrisHCl, 150 mM NaCl, pH 8.0.
    Handling Advice
    Always centrifuge tubes before opening. Do not mix by vortex or pipetting.
    Storage
    -80 °C
    Storage Comment
    Store at < -20°C, stable for 6 months after receipt.
    Please minimize freeze-thaw cycles.
    Expiry Date
    6 months
  • Target
    GLB1 (Galactosidase, beta 1 (GLB1))
    Alternative Name
    glb1 (GLB1 Products)
    Synonyms
    EBP Protein, ELNR1 Protein, MPS4B Protein, DER Protein, XR Protein, 0610038K04Rik Protein, 1810027P18Rik Protein, glb Protein, CG9092 Protein, Dmel\\CG9092 Protein, beta-GAL Protein, beta-Gal-1 Protein, beta-gal Protein, gal Protein, lacZ-1 Protein, AW125515 Protein, Bge Protein, Bgl Protein, Bgl-e Protein, Bgl-s Protein, Bgl-t Protein, Bgs Protein, Bgt Protein, C130097A14Rik Protein, BGAL Protein, zgc:110823 Protein, ECK0341 Protein, JW0335 Protein, GLB Protein, galactosidase beta 1 Protein, dicarbonyl and L-xylulose reductase Protein, dicarbonyl L-xylulose reductase Protein, beta-D-galactosidase Protein, beta-galactosidase Protein, beta galactosidase Protein, galactosidase, beta 1 Protein, beta-galactosidase-like Protein, GLB1 Protein, DCXR Protein, Dcxr Protein, lacZ Protein, SSP_RS00525 Protein, lacH Protein, ECL_03691 Protein, Gal Protein, Glb1 Protein, glb1 Protein, VV2_1327 Protein, LOC100056371 Protein
    Sub Type
    Fusionprotein
    Background
    Beta Galactosidase is a lysosomal beta Galactosidase that hydrolyzes the terminal beta Galactose from Ganglioside and Keratan sulfate. In lysosome, the mature beta Galactosidase protein associates with Cathepsin A and Neuraminidase 1 to form the lysosomal multienzyme complex . An alternative splicing at the RNA level of beta Galactosidase results a catalytically inactive beta Galactosidase that plays an important role in vascular development. Defects of beta-galactosidase (GLB1) are the cause of diseases like GM1-gangliosidosis which is a lysosomal storage disease and Morquio Syndrome B that cause patients to have abnormal elastic fibers. More than 100 mutations have been identified for beta Galactosidase, which result in different residual activities of the mutant enzymes and a spectrum of symptoms in the two related diseases.
    Alternative Names: Beta-Galactosidase, Acid Beta-Galactosidase, Lactase, Elastin Receptor 1, GLB1, ELNR1
    Molecular Weight
    74.63 kDa
    UniProt
    P16278
    Pathways
    Glycosaminoglycan Metabolic Process
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