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Anti-β-Glucocerebrosidase Antibody, clone 2I15 ZooMAb® Rabbit Monoclonal

SIGMA/ZRB1325 - recombinant, expressed in HEK 293 cells

Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-ZRB1325-25UL 25 µL
No Price  
45-ZRB1325-4X25UL 25 µL
No Price  
Immunohistochemistry (Paraffin) Enhanced Validation - Recombinant Antibody Technology Formalin Fixed Paraffin Embedded (FFPE) human liver (A) and Negative control (no primary) (B) tissue sections were prepared using heat-induced epitope retrieval (HIER). Immunostaining was performed using a 1:100 dilution of Cat. No. ZRB1325, Anti-β-Glucocerebrosidase, clone 2I15 ZooMAb® Rabbit Monoclonal. Reactivity was detected using a Goat Anti-Rabbit IgG and HRP-DAB. Cytoplasmic/membranous staining was observed in hepatocytes of human liver tissue sections.
Immunohistochemistry (Paraffin) Enhanced Validation - Recombinant Antibody Technology Formalin Fixed Paraffin Embedded (FFPE) human liver (A) and Negative control (no primary) (B) tissue sections were prepared using heat-induced epitope retrieval (HIER). Immunostaining was performed using a 1:100 dilution of Cat. No. ZRB1325, Anti-β-Glucocerebrosidase, clone 2I15 ZooMAb® Rabbit Monoclonal. Reactivity was detected using a Goat Anti-Rabbit IgG and HRP-DAB. Cytoplasmic/membranous staining was observed in hepatocytes of human liver tissue sections.
Immunohistochemistry (Paraffin) Enhanced Validation - Recombinant Antibody Technology Formalin Fixed Paraffin Embedded (FFPE) human liver (A) and Negative control (no primary) (B) tissue sections were prepared using heat-induced epitope retrieval (HIER). Immunostaining was performed using a 1:100 dilution of Cat. No. ZRB1325, Anti-β-Glucocerebrosidase, clone 2I15 ZooMAb® Rabbit Monoclonal. Reactivity was detected using a Goat Anti-Rabbit IgG and HRP-DAB. Cytoplasmic/membranous staining was observed in hepatocytes of human liver tissue sections.
Immunohistochemistry (Paraffin) Enhanced Validation - Recombinant Antibody Technology Formalin Fixed Paraffin Embedded (FFPE) human pancreas (A) and Negative control (no primary) (B) tissue sections were prepared using heat-induced epitope retrieval (HIER). Immunostaining was performed using a 1:100 dilution of Cat. No. ZRB1325, Anti-β-Glucocerebrosidase, clone 2I15 ZooMAb® Rabbit Monoclonal. Reactivity was detected using a Goat Anti-Rabbit IgG and HRP-DAB. Cytoplasmic/membranous staining was primarily observed in islets, with a lesser degree of staining observed in acinar cells of human pancreas tissue sections.
Immunohistochemistry (Paraffin) Enhanced Validation - Recombinant Antibody Technology Formalin Fixed Paraffin Embedded (FFPE) human pancreas (A) and Negative control (no primary) (B) tissue sections were prepared using heat-induced epitope retrieval (HIER). Immunostaining was performed using a 1:100 dilution of Cat. No. ZRB1325, Anti-β-Glucocerebrosidase, clone 2I15 ZooMAb® Rabbit Monoclonal. Reactivity was detected using a Goat Anti-Rabbit IgG and HRP-DAB. Cytoplasmic/membranous staining was primarily observed in islets, with a lesser degree of staining observed in acinar cells of human pancreas tissue sections.
Immunohistochemistry (Paraffin) Enhanced Validation - Recombinant Antibody Technology Formalin Fixed Paraffin Embedded (FFPE) human pancreas (A) and Negative control (no primary) (B) tissue sections were prepared using heat-induced epitope retrieval (HIER). Immunostaining was performed using a 1:100 dilution of Cat. No. ZRB1325, Anti-β-Glucocerebrosidase, clone 2I15 ZooMAb® Rabbit Monoclonal. Reactivity was detected using a Goat Anti-Rabbit IgG and HRP-DAB. Cytoplasmic/membranous staining was primarily observed in islets, with a lesser degree of staining observed in acinar cells of human pancreas tissue sections.
Immunocytochemistry Enhanced Validation - Recombinant Antibody Technology Immunofluorescent analysis of LNCaP cells was performed using a 1:100 dilution of Cat. No. ZRB1325, Anti-β-Glucocerebrosidase, clone 2I15 ZooMAb® Rabbit Monoclonal and visualized with a Goat Anti-Rabbit secondary antibody conjugated to Alexa Fluor® 488. Actin filaments have been labeled with phalloidin (Red). Nucleus is stained with DAPI (Blue). This antibody positively stains the Lysosome.
Immunocytochemistry Enhanced Validation - Recombinant Antibody Technology Immunofluorescent analysis of LNCaP cells was performed using a 1:100 dilution of Cat. No. ZRB1325, Anti-β-Glucocerebrosidase, clone 2I15 ZooMAb® Rabbit Monoclonal and visualized with a Goat Anti-Rabbit secondary antibody conjugated to Alexa Fluor® 488. Actin filaments have been labeled with phalloidin (Red). Nucleus is stained with DAPI (Blue). This antibody positively stains the Lysosome.
Immunocytochemistry Enhanced Validation - Recombinant Antibody Technology Immunofluorescent analysis of LNCaP cells was performed using a 1:100 dilution of Cat. No. ZRB1325, Anti-β-Glucocerebrosidase, clone 2I15 ZooMAb® Rabbit Monoclonal and visualized with a Goat Anti-Rabbit secondary antibody conjugated to Alexa Fluor® 488. Actin filaments have been labeled with phalloidin (Red). Nucleus is stained with DAPI (Blue). This antibody positively stains the Lysosome.
Western Blotting Enhanced Validation - Recombinant Antibody Technology HeLa (Lane 1) and LNCap (Lane 2) cell lysates were probed with Cat. No. ZRB1325, Anti-β-Glucocerebrosidase, clone 2I15 ZooMAb® Rabbit Monoclonal (1:1,000 dilution). Proteins were visualized using a Donkey Anti-Rabbit IgG secondary antibody conjugated to HRP and a chemiluminescence detection system. Arrow indicates β-Glucocerebrosidase (~60 kDa).
Affinity Binding Assay Enhanced Validation - Recombinant Antibody Technology 100 mg/mL of non-specific control peptide (Run 1) or β-Glucocerebrosidase, peptide (Run 2) were analyzed by affinity binding assay using Cat. No. ZRB1325, Anti-β-Glucocerebrosidase, clone 2I15 ZooMAb® Rabbit Monoclonal. The binding of this antibody to β-Glucocerebrosidase peptide displayed a KD of 1.0 x 10-12 whereas binding to non-specific control peptide displayed a KD of 1.2 x 10-3.
12 Principles of Green Chemistry: Principle 1—Waste Prevention.  This product has a smaller environmental footprint through reduction of waste in the manufacturing process.
12 Principles of Green Chemistry: Principle 4—Designing Safer Chemicals
Chemical products should be designed to affect their desired function while minimizing their toxicity.
12 Principles of Green Chemistry: Principle 6—Design for Energy Efficiency.  This product was re-engineered to utilize less energy in the manufacturing process.

 

antibody form purified antibody
antibody product type primary antibodies
biological source rabbit
clone 2I15, recombinant monoclonal
conjugate unconjugated
description recombinant, expressed in HEK 293 cells
enhanced validation recombinant expression
Learn more about Antibody Enhanced Validation 
epitope sequence C-terminus
form lyophilized
greener alternative category Aligned 
greener alternative product characteristics Waste Prevention
Designing Safer Chemicals
Design for Energy Efficiency
Learn more about the Principles of Green Chemistry .
isotype IgG
mol wt calculated mol wt 59.72 kDa
  observed mol wt ~60 kDa
packaging antibody small pack of 25 μL
product line ZooMAb® learn more 
Protein ID accession no. NP_000148 
Quality Level 200 
recombinant expressed in HEK 293 cells
shipped in ambient
species reactivity human
species reactivity (predicted by homology) monkey, porcine
storage temp. 2-8°C
technique(s) affinity binding assay: suitable
  immunocytochemistry: suitable
  immunohistochemistry (formalin-fixed, paraffin-embedded sections): suitable
  western blot: suitable
UniProt accession no. P04062 
Application: Quality Control Testing

Evaluated by Western Blotting in LNCap cell lysate.

Western Blotting Analysis: A 1:1,000 dilution of this antibody detected β-Glucocerebrosidase in LNCap cell lysate.

Tested applications

Western Blotting Analysis: A 1:1,000 dilution from a representative lot detected β-Glucocerebrosidase in HeLa cell lysate.

Immunohistochemistry (Paraffin) Analysis: A 1:100 dilution from a representative lot detected β-Glucocerebrosidase in human liver and human pancreas tissue sections.

Immunocytochemistry Analysis: A 1:100 dilution from a representative lot detected β-Glucocerebrosidase in LNCaP cells.

Affinity Binding Assay: A representative lot of this antibody bound β-Glucocerebrosidase peptide with a KD of 1.0 x 10-12 in an affinity binding assay.

Note: Actual optimal working dilutions must be determined by end user as specimens, and experimental conditions may vary with the end user
Application: Anti-β-Glucocerebrosidase, clone 2I15 ZooMAb®, Cat. No. ZRB1325, is a recombinant Rabbit monoclonal antibody that detects β-Glucocerebrosidase and is tested for use in Affinity Binding Assay, Immunocytochemistry, Immunohistochemistry & Western Blotting.
Disclaimer: Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
General description: We are committed to bringing you greener alternative products, which adhere to one or more of The 12 Principles of Green Chemistry.This antibody is Preservative-free, produced without the harm or sacrifice of animals and exceptionally stable to allow for ambient shipping and storage if needed and thus aligns with "Waste Prevention", "Designing Safer Chemicals" and "Design for Energy Efficiency". Click here  for more information.
General description: ZooMAb® antibodies represent an entirely new generation of recombinant monoclonal antibodies.

Each ZooMAb® antibody is manufactured using our proprietary recombinant expression system, purified to homogeneity, and precisely dispensed to produce robust and highly reproducible lot-to-lot consistency. Only top-performing clones are released for use by researchers. Each antibody is validated for high specificity and affinity across multiple applications, including its most commonly used application. ZooMAb® antibodies are reliably available and ready to ship when you need them.

Learn more about ZooMAb here. 
Immunogen: KLH-conjugated linear peptide corresponding to 20 amino acids from the C-terminal region of human β-Glucocerebrosidase.
Legal Information: ZooMAb is a registered trademark of Merck KGaA, Darmstadt, Germany
Physical form: Purified recombinant rabbit monoclonal antibody IgG, lyophilized in PBS with 5% Trehalose, normal appearance a coarse or translucent resin. The PBS/trehalose components in the ZooMAb formulation can have the appearance of a semi-solid (bead like gel) after lyophilization. This is a normal phenomenon. Please follow the recommended reconstitution procedure in the data sheet to dissolve the semi-solid, bead-like, gel-appearing material. The resulting antibody solution is completely stable and functional as proven by full functional testing. Contains no biocide or preservatives, such as azide, or any animal by-products. Larger pack sizes provided as multiples of 25 μL.
Reconstitution: 300 μg/mL after reconstitution at 25 μL per vial. Please refer to guidance on suggested starting dilutions and/or titers per application and sample type.
Specificity: Clone 2I15 is a ZooMAb® rabbit recombinant monoclonal antibody that specifically detects β-Glucocerebrosidase. It targets an epitope within 20 amino acids from the C-terminal region.
Storage and Stability: Recommend storage of lyophilized product at 2-8°C; Before reconstitution, micro-centrifuge vials briefly to spin down material to bottom of the vial; Reconstitute each vial by adding 25 μL of filtered lab grade water or PBS; Reconstituted antibodies can be stored at 2-8°C, or -20°C for long term storage. Avoid repeated freeze-thaws.
Target description: Lysosomal acid glucosylceramidase (UniProt: P04062; also known as EC:3.2.1.45; Lysosomal acid GCase, Acid beta-glucosidase, Alglucerase, Beta-glucocerebrosidase, Beta-GC, Cholesterol glucosyltransferase, SGTase, Cholesteryl-beta-glucosidase, D-glucosyl-N-acylsphingosine glucohydrolase, Imiglucerase) is encoded by the GBA (also known as GC, GLUC) gene (Gene ID: 2629) in human. β-Glucocerebrosidase is a peripheral membrane glycoprotein that catalyzes the hydrolysis of glucosylceramide/GlcCer into free ceramide and glucose in the lysosomal compartment. It is shown to be maximally active at pH 5.5. Within the lysosome, it remains associated with the membrane, where it binds and degrades its substrate. Its interaction with saposin-C is reported to promote its membrane association. It plays a key role in the degradation of complex lipids and the turnover of cellular membranes. Through the production of ceramides, it participates in the PKC-activated salvage pathway of ceramide formation. It is also reported to plays a role in cholesterol metabolism and can catalyze the glucosylation of cholesterol, through a transglucosylation reaction that transfers glucose from glucosylceramide to cholesterol. Mutations in GBA gene are shown to cause Gaucher disease, a lysosomal storage disease characterized by accumulation of glucosylceramide in the reticulo-endothelial system. GBA mutations are also shown to be the strongest known risk factor for the development of Parkinson s disease. Five isoforms of β-Glucocerebrosidase have been described that are produced by alternative splicing. This ZooMAb® recombinant monoclonal antibody, generated by our propriety technology, offers significantly enhanced specificity, affinity, reproducibility, and stability over conventional monoclonals.
WGK Germany WGK 1
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Storage Temp. 2-8°C

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