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Human TJP2 / ZO2 / ZO-2 Protein (Recombinant His + T7) (aa307-669) - LS-G25560

Catalog Size Price
LS-G25560-10 10 µg Unavailable
LS-G25560-50 50 µg Unavailable
LS-G25560-100 100 µg Unavailable
LS-G25560-200 200 µg Unavailable

Most Popular TJP2 / ZO2 / ZO-2 Proteins

Human TJP2 / ZO2 / ZO-2 Protein (Recombinant His + T7) (aa307-669) - LS-G25560
E. coli Expression System
His + T7
Human TJP2 / ZO2 / ZO-2 Protein (Recombinant GST,N-terminus) (aa121-218) - LS-G61113
Wheat Wheat Germ Extract
98 AA
12.5% SDS-PAGE Stained with Coomassie Blue.
Human TJP2 / ZO2 / ZO-2 Protein (Recombinant Myc + DDK) - LS-G67992
Human HEK 293 Cells
1242 AA
Myc + DDK
Purified recombinant protein TJP2 was analyzed by SDS-PAGE gel and Coomassie Blue Staining
Human TJP2 / ZO2 / ZO-2 Protein (Over-Expression Lysate Myc + DDK) - LS-G81184
Human 293T Cells
1242 AA
Myc + DDK
Purified / Lyophilized
Western validation with an anti-DDK antibody * L: Control HEK293 lysate R: Over-expression lysate
TJP2 / ZO2 / ZO-2 Protein (Over-Expression Lysate Myc + DDK) - LS-G100397
Human HEK 293 Cells
1242 AA
Myc + DDK
Western validation with an anti-DDK antibody * L: Control HEK293 lysate R: Over-expression lysate

100% Guaranteed
Recombinant Protein
TJP2 / ZO2 / ZO-2
44.2 kDa
aa 307-669
E. coli
E. coli
His + T7
Not Tested
Not Tested
Lyophilized from PBS, pH 7.4, 0.01% Sarcosyl, 1 mM DTT, 5% Trehalose, Proclin300.
Store at 4°C for up to 1 month, or aliquot and store at -80°C for up to 1 year. Avoid freeze-thaw cycles.
For research use only.

About TJP2 / ZO2 / ZO-2

Q9UDY2 NM_004817 NP_004808.2

TJP2 Protein, C9DUPq21.11 Protein, DUP9q21.11 Protein, DFNA51 Protein, ZO-2 Protein, Zona occludens 2 Protein, Zonula occludens protein 2 Protein, Tight junction protein 2 Protein, Tight junction protein ZO-2 Protein, ZO2 Protein, X104 Protein, Zona occludens protein 2 Protein

TJP2 / ZO2 / ZO-2 is a zonula occluden that is a member of the membrane-associated guanylate kinase homolog family. The encoded protein functions as a component of the tight junction barrier in epithelial and endothelial cells and is necessary for proper assembly of tight junctions. Mutations in this gene have been identified in patients with hypercholanemia, and genomic duplication of a 270 kb region including this gene causes autosomal dominant deafness-51.

Requested From: 
Date Requested: 6/21/2018

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