GLB1 Protein (His tag)

Catalog No. ABIN7319218

Product Details

Target: GLB1 (Galactosidase, beta 1 (GLB1))

Protein Type: Recombinant

Origin: Human

Source: Human Cells

Purification tag / Conjugate: This GLB1 protein is labelled with His tag.

Purpose: Recombinant Human β-Galactosidase/GLB1 Protein (His Tag)

Sequence: Leu24-Val677

Characteristics: Recombinant Human beta-Galactosidase is produced by our Mammalian expression system and the target gene encoding Leu24-Val677 is expressed with a 6His tag at the C-terminus.

Purity: > 95 % as determined by reducing SDS-PAGE.

Endotoxin Level: < 1.0 EU per μg as determined by the LAL method.

Application Details

Restrictions: For Research Use only

Handling

Format: Frozen, Liquid

Buffer: Supplied as a 0.2 μm filtered solution of 20 mM TrisHCl, 150 mM NaCl, pH 8.0.

Storage: -20 °C

Storage Comment: Store at < -20°C, stable for 6 months. Please minimize freeze-thaw cycles.

Target Details

Target: GLB1 (Galactosidase, beta 1 (GLB1))

Alternative Name: beta-Galactosidase/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

Background:

Background: β Galactosidase is a lysosomal β Galactosidase that hydrolyzes the terminal β Galactose from Ganglioside and Keratan sulfate. In lysosome, the mature β Galactosidase protein associates with Cathepsin A and Neuraminidase 1 to form the lysosomal multienzyme complex . An alternative splicing at the RNA level of β Galactosidase results a catalytically inactive β Galactosidase that plays an important role in vascular development. Defects of β-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 β Galactosidase, which result in different residual activities of the mutant enzymes and a spectrum of symptoms in the two related diseases.

Synonym: Beta-Galactosidase, Acid Beta-Galactosidase, Lactase, Elastin Receptor 1, GLB1, ELNR1

Molecular Weight: 74.6 kDa

UniProt: P16278

Pathways: Glycosaminoglycan Metabolic Process