PIPA525737

GM2A Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA525737-Each-of-1 In Stock ₹ 47,036.50

PIPA525737 - Each of 1

₹ 47,036.50

In Stock

Quantity

1

Base Price: ₹ 47,036.50

GST (18%): ₹ 8,466.57

Total Price: ₹ 55,503.07

Antigen

GM2A

Classification

Polyclonal

Formulation

PBS with 0.09% sodium azide

Gene Accession No.

P17900, Q60648

Gene Symbols

GM2A

Immunogen

KLH conjugated synthetic peptide between 25-54 amino acids from the N-terminal region of human GM2A

Quantity

400 μL

Primary or Secondary

Primary

Target Species

Human, Mouse

Product Type

Antibody

Isotype

IgG

Applications

Western Blot

Conjugate

Unconjugated

Gene

GM2A

Gene Alias

AA408702; AW215435; cerebroside sulfate activator protein; Ganglioside GM2 activator; Ganglioside GM2 activator isoform short; GM2 ganglioside activator; GM2 ganglioside activator protein; Gm2a; GM2-AP; SAP-3; shingolipid activator protein 3; sphingolipid activator protein 3

Host Species

Rabbit

Purification Method

Antigen affinity chromatography, Protein A

Regulatory Status

RUO

Gene ID (Entrez)

14667, 2760

Content And Storage

-20° C, Avoid Freeze/Thaw Cycles

Form

Liquid

Related Products

Img

Thermo Scientific

PIPA525329

--

Img

Thermo Scientific

PIPA525543

--

Img

Thermo Scientific

PIPA526572

--

Img

Thermo Scientific

PIPA526580

--

Img

Thermo Scientific

PIPA526791

--

Img

Thermo Scientific

PIPA526509

--

Img

Thermo Scientific

PIPA525727

--

Img

Thermo Scientific

PIPA526250

--

Description

  • This antibody is predicted to react with non-human primate based on sequence homology
  • This gene encodes a small glycolipid transport protein which acts as a substrate specific co-factor for the lysosomal enzyme beta-hexosaminidase A
  • Beta-hexosaminidase A, together with GM2 ganglioside activator, catalyzes the degradation of the ganglioside GM2, and other molecules containing terminal N-acetyl hexosamines
  • Mutations in this gene result in GM2-gangliosidosis type AB or the AB variant of Tay-Sachs disease
  • Alternative splicing results in multiple transcript variants.