SOX2 Antilichaam

This intronless gene encodes a member of the SRY-related HMG-box (SOX) family of transcription factors involved in the regulation of embryonic development and in the determination of cell fate. The product of this gene is required for stem-cell maintenance in the central nervous system, and also regulates gene expression in the stomach. Mutations in this gene have been associated with optic nerve hypoplasia and with syndromic microphthalmia, a severe form of structural eye malformation. This gene lies within an intron of another gene called SOX2 overlapping transcript (SOX2OT) .

6657

P48431

Human, Mouse, Rat

Recombinant fusion protein containing a sequence corresponding to amino acids 1-140 of human SOX2 (NP_003097.1) .

Unconjugated

Primary Antibodies

Cell Cycle, Neuroscience, Signal Transduction, Stem Cell, Transcription

Affinity purification

MCF7

Batch dependent

PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

None

Blue Ice

Store at -20˚ C. Avoid freeze / thaw cycles.

Observed: 39kDa

IgG

SOX2

293T

Mouse brain

Rat brain

SRY (sex determining region Y) -box 2

Homo sapiens

SOX2 Antibody: ANOP3, MCOPS3, Transcription factor SOX-2

WB, IHC, IF, IP

Liquid