Recombinant GFAP Monoklonale Antilichaam

GFAP (Glial fibrillary acidic protein) is a type III intermediate filament protein. It is the major component of astrocyte intermediate filament. Defects in GFAP are a cause of Alexander disease. Alexander disease is a rare disorder of the central nervous system. It is a progressive leukoencephalopathy whose hallmark is the widespread accumulation of Rosenthal fibers which are cytoplasmic inclusions in astrocytes. At the amino acid sequence level, human GFAP shares 91% and 90% identity with rat and mouse GFAP, respectively.

GFAP

P14136

Human

A synthetic peptide corresponding to the center region of the human GFAP

ZGC; etID36982; wu:fb34h; wu:fk42c; ALXDRD; GFAP; cb345; etID36982.3; FLJ42474; FLJ45472; gfapl; Glial Fibrillary Acidic Protein; Intermediate Filament Protein; wu:fb34h11; wu:fk42c12; xx:af506734; zgc:110485; wu:fb34h11; ALXDRD; cb345; etID36982.3; FLJ42474; FLJ45472; GFAP; GFAP; gfapl; Glial fibrillary acidic protein; Intermediate filament protein; wu:fk42c12; xx:af506734; zgc:110485

4B2

Unconjugated

WB

Neuroscience; Signal Transduction; Tags & Cell Markers; Stem Cells

Protein A

1 mg/mL

WB 1:500-1:1000

0.2 μm filtered solution in PBS

Ice bag

This antibody can be stored at 2°C-8°C for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20°C to -80°C. Preservative-Free. Avoid repeated freeze-thaw cycles.

https://789.bio/eb/YqWZRSEO

50 kDa

45 kDa

IgG