LAMB3 Antilichaam

The product encoded by this gene is a laminin that belongs to a family of basement membrane proteins. This protein is a beta subunit laminin, which together with an alpha and a gamma subunit, forms laminin-5. Mutations in this gene cause epidermolysis bullosa junctional Herlitz type, and generalized atrophic benign epidermolysis bullosa, diseases that are characterized by blistering of the skin. Multiple alternatively spliced transcript variants that encode the same protein have been found for this gene.

3914

Q13751

Rat

Recombinant fusion protein containing a sequence corresponding to amino acids 18-230 of human LAMB3 (NP_000219.2) .

Unconjugated

Primary Antibodies

Other

Affinity purification

Rat liver

Batch dependent

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

None

Blue Ice

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

Observed: 131kDa

IgG

WB: 1:500 - 1:2000

LAMB3

Laminin subunit beta 3

Homo sapiens

AI1A, BM600-125KDA, LAM5, LAMNB1, laminin subunit beta-3, epiligrin subunit bata, kalinin B1 chain, kalinin subunit beta, kalinin-140kDa, laminin B1k chain, laminin S B3 chain, laminin beta 3, laminin, beta 3 (nicein (125kD), kalinin (140kD), BM600 (125kD) ), laminin-5 subunit beta, nicein subunit beta, nicein-125kDa

WB

Liquid