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Anti-Galactosidase alpha Rabbit Monoclonal Antibody

Catalog No.
MA2740
Anti-Galactosidase alpha Rabbit Monoclonal Antibody
Grouped product items
SizePriceStock Qty
50ul
$210.00
Ship with 3-5 days
100ul
$375.00
Ship with 3-5 days
For scientific research use only and should not be used for diagnostic or medical purposes.

Tel: +1-832-696-8203

Email: [email protected]

Worldwide Distributors

Background

Defects in GLA are the cause of Fabry disease (FD) [MIM:301500]. FD is a rare X-linked sphingolipidosis disease where glycolipid accumulates in many tissues. The disease consists of an inborn error of glycosphingolipid catabolism.

Quality Control

Quality Control & MSDS

View current batch:
 

Gene ID

2717

Alternative Names

Alpha gal A; GALA; Galactosidase; alpha; GLA; Melibiase

Host

Rabbit

Reactivity

Human

Conjugation

Unconjugated

M.Wt

Calculated MW: 49 kDa; Observed MW: 49 kDa

Modification

Unmodified

Isotype

IgG

Clonality

Monoclonal Antibody

Clonality No.

AP-13F12B10

Form

Liquid

Concentration

See label

Carrier

Carrier Not Free

Immunogen

A synthetic peptide of human Galactosidase alpha

Purification

Affinity Purified

Buffer System

50mM Tris-Glycine (pH 7.4), 0.15M NaCl, 40% Glycerol, 0.01% Sodium azide and 0.05% BSA.

Application

WB, IHC-P, IP

Shipping Condition

Blue ice

Storage

-20°C

Expiration Date

12 months

Note

Please avoid freeze-thaw cycles.