USP9X Antibody

Product Specifications

Background

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.

NCBI Gene ID

8239

Swiss Prot

Q93008

Host

Rabbit

Reactivity

Human, Mouse, Rat

Immunogen

A synthetic peptide of human USP9X

Clonality

Polyclonal

Conjugation

Unconjugated

Type

Primary Antibodies

Field of Research

Cell Cycle, Neuroscience

Purification

Affinity purification

Positive Control

293T

Concentration

Batch dependent

Buffer

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

Modification

None

Shipping Conditions

Blue Ice

Storage Conditions

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

Calculated Molecular Weight

Observed: 292kDa

Fragment

IgG

Applications Notes

WB: 1:500 - 1:2000

Symbol

USP9X

Positive Control 2

U-251MG

Positive Control 3

Positive Control 4

Mouse brain

NCBI Official Name

Ubiquitin specific peptidase 9 X-linked

NCBI Organism

Homo sapiens

Other Product Names

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