Glucosidase IIβ Polyclonal Antibody

Rabbit Anti-Glucosidase IIβ Polyclonal Antibody

Product Specifications

Background

PRKCSH encodes the beta-subunit of glucosidase II, an N-linked glycan-processing enzyme in the endoplasmic reticulum. Glucosidase 2 subunit beta is an acidic phosphoprotein known to be a substrate for protein kinase C. Mutations in PRKCSH have been associated with the autosomal dominant polycystic liver disease. Alternative splicing results in multiple transcript variants.

CAS Number

9007-83-4

Product Name Alternative

PRKCSH; G19P1; Glucosidase 2 subunit beta; 80K-H protein; Glucosidase II subunit beta; Protein kinase C substrate 60.1 kDa protein heavy chain; PKCSH

Gene ID

5589

Accession Number

P14314

Reactivity

Human, Mouse

Immunogen

Synthesized peptide derived from the Internal region of human Glucosidase IIβ at AA range: 50-130

Clonality

Polyclonal

Tag

Glucosidase 2 subunit beta

Applications

WB, IF, ELISA

Purification Method

The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Concentration

1 mg/ml

Molecular Weight

59kD

Precautions

The product listed herein is for research use only and is not intended for use in human or clinical diagnosis. Suggested applications of our products are not recommendations to use our products in violation of any patent or as a license. We cannot be responsible for patent infringements or other violations that may occur with the use of this product.

Shipping Conditions

Gel pack with blue ice.

Storage Conditions

Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Notes

Glucosidase IIβ Polyclonal Antibody detects endogenous levels of Glucosidase IIβ protein.

Observed Molecular Weight

Formulation

Liquid solution

Buffer pH

Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

Applications Notes

Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-1:2000; IF 1:200-1:1000; ELISA 1:10000; Not yet tested in other applications.