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UB2Q1 Polyclonal Antibody, 20ul Cell Transfection This autosomal dominant disorder is

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UB2Q1 Polyclonal Antibody, 20ul Cell Transfection This autosomal dominant disorder isThe modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin activating enzymes (E1s), ubiquitin conjugating enzymes (E2s), and ubiquitin protein ligases (E3s). This gene encodes a member of the E2 ubiquitin conjugating enzyme family. The encoded protein is 98% identical to the mouse counterpart.

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Description

This autosomal dominant disorder is characterized by abnormal water reabsorption by kidney tubules due

which may occur via its interaction with AIF

H+ transporting

It is expressed in the tissue and circulating myeloid leukocytes

The full-length nature of variants which differ in repeat length has not been determined

UB2Q1 Polyclonal Antibody, 20ul Cell Transfection This autosomal dominant disorder isThe modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin activating enzymes (E1s), ubiquitin conjugating enzymes (E2s), and ubiquitin protein ligases (E3s). This gene encodes a member of the E2 ubiquitin conjugating enzyme family. The encoded protein is 98% identical to the mouse counterpart.

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