USP9X Antilichaam

This gene is a member of the peptidase C19 family and encodes a protein that is similar to ubiquitin-specific proteases. Though this gene is located on the X chromosome, it escapes X-inactivation. Mutations in this gene have been associated with Turner syndrome. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.

8239

Q93008

Human, Mouse, Rat

A synthetic peptide of human USP9X

Unconjugated

Primary Antibodies

Cell Cycle, Neuroscience

Affinity purification

293T

Batch dependent

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

None

Blue Ice

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

Observed: 292kDa

IgG

WB: 1:500 - 1:2000

USP9X

U-251MG

C6

Mouse brain

Ubiquitin specific peptidase 9 X-linked

Homo sapiens

DFFRX, FAF, FAM, MRX99, MRXS99F, probable ubiquitin carboxyl-terminal hydrolase FAF-X, Drosophila fat facets related, X-linked, deubiquitinating enzyme FAF-X, fat facets in mammals, fat facets protein related, X-linked, hFAM, ubiquitin specific protease 9, X chromosome (fat facets-like Drosophila), ubiquitin thioesterase FAF-X, ubiquitin thiolesterase FAF-X, ubiquitin-specific processing protease FAF-X, ubiquitin-specific protease 9, X chromosome

WB

Liquid