PIPA530097

NAGLU Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA530097-Each-of-1 In Stock ₹ 49,617.50

PIPA530097 - Each of 1

₹ 49,617.50

In Stock

Quantity

1

Base Price: ₹ 49,617.50

GST (18%): ₹ 8,931.15

Total Price: ₹ 58,548.65

Antigen

NAGLU

Classification

Polyclonal

Conjugate

Unconjugated

Gene

NAGLU

Gene Alias

Alpha-N-acetylglucosaminidase; alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB); Alpha-N-acetylglucosaminidase 77 kDa form; Alpha-N-acetylglucosaminidase 82 kDa form; alpha-N-acetylglucosaminidase, lysosomal; CMT2V; MPS3B; MPS-IIIB; N-acetyl-alpha-glucosaminidase; N-acetyl-glucosaminidase; N-acetylglucosaminidase, alpha; NAG; NAGLU; RGD1564228; testicular tissue protein Li 18; UFHSD; UFHSD1

Host Species

Rabbit

Purification Method

Antigen affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

27419, 360630, 4669

Content And Storage

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

Form

Liquid

Applications

Immunocytochemistry, Immunohistochemistry (Paraffin), Western Blot

Concentration

1 mg/mL

Formulation

0.1M tris glycine with 20% glycerol and 0.01% thimerosal; pH 7

Gene Accession No.

P54802

Gene Symbols

NAGLU

Immunogen

Recombinant fragment corresponding to a region within amino acids 252 and 487 of Human NAGLU

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human, Mouse, Rat

Product Type

Antibody

Isotype

IgG

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Description

  • Recommended positive controls: U87-MG, SK-N-SH, IMR32, SK-N-AS, mouse brain, rat brain
  • Predicted reactivity: Mouse (87%), Bovine (90%)
  • Store product as a concentrated solution
  • Centrifuge briefly prior to opening the vial
  • This gene encodes an enzyme that degrades heparan sulfate by hydrolysis of terminal N-acetyl-D-glucosamine residues in N-acetyl-alpha-D-glucosaminides
  • Defects in this gene are the cause of mucopolysaccharidosis type IIIB (MPS-IIIB), also known as Sanfilippo syndrome B
  • This disease is characterized by the lysosomal accumulation and urinary excretion of heparan sulfate.