PIPA521375

SGSH Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA521375-Each-of-1 In Stock ₹ 49,350.50

PIPA521375 - Each of 1

₹ 49,350.50

In Stock

Quantity

1

Base Price: ₹ 49,350.50

GST (18%): ₹ 8,883.09

Total Price: ₹ 58,233.59

Antigen

SGSH

Classification

Polyclonal

Conjugate

Unconjugated

Gene

SGSH

Gene Alias

4632406A19Rik; heparan sulfate sulfamidase; heparan sulfate sulfatase; HSS; MPS3A; mucopolysaccharidosis type IIIA; N-sulfoglucosamine sulfohydrolase; N-sulfoglucosamine sulfohydrolase (sulfamidase); N-sulphoglucosamine sulphohydrolase; SFMD; SGSH; Sulfoglucosamine sulfamidase; sulphamidase

Host Species

Rabbit

Purification Method

Protein A

Regulatory Status

RUO

Gene ID (Entrez)

6448

Content And Storage

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

Form

Liquid

Applications

Western Blot

Concentration

2 mg/mL

Formulation

PBS with 40% glycerol and 0.01% thimerosal; pH 7

Gene Accession No.

P51688

Gene Symbols

SGSH

Immunogen

Recombinant fragment corresponding to a region within amino acids 44 and 230 of SGSH (Uniprot ID#P51688)

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human

Product Type

Antibody

Isotype

IgG

Related Products

Img

Thermo Scientific

PIPA521374

--

Img

Thermo Scientific

PIPA526584

--

Img

Thermo Scientific

PIPA527389

--

Img

Thermo Scientific

PIPA527403

--

Img

Thermo Scientific

PIPA527397

--

Img

Thermo Scientific

PIPA521425

--

Img

Thermo Scientific

PIPA527428

--

Img

Thermo Scientific

PIPA521385

--

Description

  • Recommended positive controls: 293T
  • Predicted reactivity: Mouse (93%), Dog (92%), Bovine (90%)
  • Store product as a concentrated solution
  • Centrifuge briefly prior to opening the vial
  • SGSH is one of several enzymes involved in the lysosomal degradation of heparan sulfate
  • Mutations in this gene are associated with Sanfilippo syndrome A, one type of the lysosomal storage disease mucopolysaccaridosis III, which results from impaired degradation of heparan sulfate
  • Transcripts of varying sizes have been reported but their biological validity has not been determined.