50-173-1204

GFAP Rabbit anti-Human, Mouse, Rat, Polyclonal, Proteintech

Manufacturer: Proteintech Group Inc

Select a Size

Pack Size SKU Availability Price
Each of 1 50-173-1204-Each-of-1 In Stock ₹ 44,150.23

50-173-1204 - Each of 1

₹ 44,150.23

In Stock

Quantity

1

Base Price: ₹ 44,150.23

GST (18%): ₹ 7,947.041

Total Price: ₹ 52,097.271

Antigen

GFAP

Classification

Polyclonal

Conjugate

Unconjugated

Gene

GFAP

Gene Alias

GFAP

Host Species

Rabbit

Purification Method

Antigen Affinity Chromatography

Regulatory Status

RUO

Gene ID (Entrez)

14580, 24387, 2670

Content And Storage

-20°C

Form

Liquid

Applications

Immunocytochemistry, Immunofluorescence, Immunohistochemistry (Paraffin), Western Blot

Concentration

0.43 mg/mL

Formulation

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

Gene Accession No.

P03995, P14136, P47819

Gene Symbols

Gfap

Immunogen

GFAP Fusion Protein Ag10423

Quantity

150 μL

Primary or Secondary

Primary

Target Species

Human, Mouse, Rat

Product Type

Antibody

Isotype

IgG

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Description

  • GFAP (Glial fibrillary acidic protein) is a member of the class III intermediate filament protein family
  • GFAP is heavily, and specifically, expressed in astrocytes and certain astroglia in the central nervous system, in satellite cells in peripheral ganglia, and in non-myelinating Schwann cells in peripheral nerves
  • In addition, neural stem cells strongly express GFAP
  • Antibodies to GFAP are very useful as markers of astrocytic cells
  • In addition, many types of brain tumor, presumably derived from astrocytic cells, heavily express GFAP
  • GFAP is also found in the lens epithelium, Kupffer cells of the liver, in some cells in salivary tumors and has been reported in erythrocytes
  • GFAP is used as a marker to distinguish astrocytes from other glial cells during development
  • Mutations in this gene cause Alexander disease, a rare disorder of astrocytes in the central nervous system
  • Alternative splicing of the GFAP gene results in multiple transcript variants encoding distinct isoforms.