NDE1 Antilichaam

This gene encodes a member of the nuclear distribution E (NudE) family of proteins. The encoded protein is localized at the centrosome and interacts with other centrosome components as part of a multiprotein complex that regulates dynein function. This protein plays an essential role in microtubule organization, mitosis and neuronal migration. Mutations in this gene cause lissencephaly 4, a disorder characterized by lissencephaly, severe brain atrophy, microcephaly, and severe mental retardation. Alternative splicing results in multiple transcript variants.

54820

Q9NXR1

Human, Mouse

Recombinant fusion protein containing a sequence corresponding to amino acids 1-110 of human NDE1 (NP_060138.1) .

Unconjugated

Primary Antibodies

Cell Cycle, Neuroscience

Affinity purification

HeLa

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

NDE1

HepG2

Mouse spleen

NudE neurodevelopment protein 1

Homo sapiens

NDE1, FLJ20101, HOM-TES-87, NUDE, NUDE1, NDE, LIS4

WB, IF

Liquid