Thermo Fisher Scientific alpha Galactosidase Polyclonal Antibody

Applications

Tested Dilution

Publications

Western Blot (WB)

1:1,000-1:5,000

View 1 publication 1 publication

ELISA (ELISA)

1:1,000-1:5,000

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Product Specifications

Species Reactivity

Human

Published species

Bacteria

Host/Isotype

Chicken / IgY

Class

Polyclonal

Type

Antibody

Immunogen

Mix of synthetic peptides corresponding to residues 55-64 and 396-407 of human alpha Galactosidase if (typeof window.$mangular === undefined || !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{targetFamily:alpha Galactosidase,uniProtId:P06280-1,ncbiNodeId:9606,antigenRange:55-64|396-407,antigenLength:429,antigenImageFileName:PA1-9528_alpha_Galactosidase_P06280-1_Chicken.svg,antigenImageFileNamePDP:PA1-9528_alpha_Galactosidase_P06280-1_Chicken_PDP.jpeg,sortOrder:1}\]; $mangular.isB2BCMGT = false; $mangular.isEpitopesModalImageMultiSizeEnabled = true;

View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}

Conjugate

Unconjugated Unconjugated Unconjugated

Form

Liquid

Concentration

1 mg/mL

Purification

IgY fraction

Storage buffer

PBS

Contains

0.02% sodium azide

Storage conditions

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

Shipping conditions

Ambient (domestic); Wet ice (international)

RRID

AB_2263438

Product Specific Information

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.

Target Information

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.

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.