PIMA535650

alpha Galactosidase Recombinant Rabbit Monoclonal Antibody (ARC1213), Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIMA535650-Each-of-1 In Stock ₹ 47,481.50

PIMA535650 - Each of 1

₹ 47,481.50

In Stock

Quantity

1

Base Price: ₹ 47,481.50

GST (18%): ₹ 8,546.67

Total Price: ₹ 56,028.17

Antigen

alpha Galactosidase

Classification

Monoclonal

Concentration

1.23 mg/mL

Formulation

PBS with 0.05% BSA, 50% glycerol and 0.02% sodium azide; pH 7.3

Gene Accession No.

P06280, P51569

Gene Symbols

GLA

Immunogen

A synthetic peptide corresponding to a sequence within amino acids 50-150 of human Galactosidase alpha (GLA) (GLA) (P06280)

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human, Mouse, Rat

Product Type

Antibody

Isotype

IgG

Applications

Western Blot

Clone

ARC1213

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

Rabbit

Purification Method

Affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

11605, 2717, 363494

Content And Storage

-20° C, Avoid Freeze/Thaw Cycles

Form

Liquid

Related Products

Img

Novus Biologicals

NB317023

--

Img

Novus Biologicals

NB317032

--

Img

Thermo Scientific

PIMA531619

--

Img

Thermo Scientific

PIPA5120391

--

Img

Thermo Scientific

PIPA5103475

--

Img

Thermo Scientific

PIMA514921

--

Img

Thermo Scientific

PIMA536095

--

Img

Thermo Scientific

PIPA596651

--

Description

  • Immunogen sequence: FMCNLDCQEE PDSCISEKLF MEMAELMVSE GWKDAGYEYL CIDDCWMAPQ RDSEGRLQAD PQRFPHGIRQ LANYVHSKGL KLGIYADVGN KTCAGFPGSF G 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.