01-674-411

alpha Galactosidase Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 01-674-411-Each-of-1 In Stock ₹ 40,851.00

01-674-411 - Each of 1

₹ 40,851.00

In Stock

Quantity

1

Base Price: ₹ 40,851.00

GST (18%): ₹ 7,353.18

Total Price: ₹ 48,204.18

Antigen

alpha Galactosidase

Classification

Polyclonal

Conjugate

Unconjugated

Gene

GLA

Gene Alias

Agalsidase; agalsidase alfa; Ags; Alpha-D-galactosidase A; alpha-D-galactoside galactohydrolase; alpha-D-galactoside galactohydrolase 1; alpha-gal A; alpha-galactosidase A; GALA; galactosidase alpha; galactosidase, alpha; GLA; Melibiase

Host Species

Chicken

Purification Method

IgY fraction

Regulatory Status

RUO

Gene ID (Entrez)

2717

Content And Storage

Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.

Form

Liquid

Applications

ELISA, Western Blot

Concentration

1 mg/mL

Formulation

PBS with 0.02% sodium azide

Gene Accession No.

P06280

Gene Symbols

GLA

Immunogen

Mix of synthetic peptides corresponding to residues 55-64 and 396-407 of human alpha Galactosidase

Quantity

500 μg

Primary or Secondary

Primary

Target Species

Human

Product Type

Antibody

Isotype

IgY

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Description

  • PA1-9528 detects Alpha Galactosidase in human samples
  • PA1-9528 has been successfully used in Western blot and ELISA procedures
  • The PA1-9528 immunogen is a mix of synthetic peptides corresponding to residues 55-64 and 396-407 of human alpha Galactosidase
  • Store at 4oC for one week, and -20oC for long term storage
  • This gene encodes a homodimeric glycoprotein that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins
  • This enzyme predominantly hydrolyzes ceramide trihexoside, and it can catalyze the hydrolysis of melibiose into galactose and glucose
  • A variety of mutations in this gene affect the synthesis, processing, and stability of this enzyme, which causes Fabry disease, a rare lysosomal storage disorder that results from a failure to catabolize alpha-D-galactosyl glycolipid moieties.