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POMT2 Rabbit Polyclonal Antibody, 50ul Sample Library Tubes corneal dystrophy and perceptive deafness

SKU: 4045250962

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USD185.00 USD217.00

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POMT2 Rabbit Polyclonal Antibody, 50ul Sample Library Tubes corneal dystrophy and perceptive deafnessThe protein encoded by this gene is an O mannosyltransferase that requires interaction with the product of the POMT1 gene for enzymatic function. The encoded protein is found in the membrane of the endoplasmic reticulum. Defects in this gene are a cause of Walker Warburg syndrome (WWS).

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Description

corneal dystrophy and perceptive deafness

which catalyzes production of lysophosphatidic acid (LPA) in extracellular fluids

a key cytokine involved in inflammation and immune responses

An important paralog of RAB35 is HRAS

and the T-cell receptor on the T lymphocyte recognize antigens displayed by an antigen presenting cell (APC) in the context of class I MHC molecules

POMT2 Rabbit Polyclonal Antibody, 50ul Sample Library Tubes corneal dystrophy and perceptive deafnessThe protein encoded by this gene is an O mannosyltransferase that requires interaction with the product of the POMT1 gene for enzymatic function. The encoded protein is found in the membrane of the endoplasmic reticulum. Defects in this gene are a cause of Walker Warburg syndrome (WWS).

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