STOM-antilichaam

This gene encodes a member of a highly conserved family of integral membrane proteins. The encoded protein localizes to the cell membrane of red blood cells and other cell types, where it may regulate ion channels and transporters. Loss of localization of the encoded protein is associated with hereditary stomatocytosis, a form of hemolytic anemia. There is a pseudogene for this gene on chromosome 6. Alternative splicing results in multiple transcript variants.

2040

P27105

Human, Mouse, Rat

Recombinant fusion protein containing a sequence corresponding to amino acids 55-288 of human STOM (NP_004090.4) .

Unconjugated

Primary Antibodies

Neuroscience

Affinity purification

A-549

Batch dependent

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

None

Blue Ice

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

Observed: 36kDa

IgG

WB: 1:500 - 1:2000

STOM

U-251MG

BxPC-3

STOM

Homo sapiens

STOM, stomatin, BND7, EPB7, EPB72, erythrocyte band 7 integral membrane protein, erythrocyte membrane protein band 7.2 (stomatin), protein 7.2b

WB

Liquid