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ATS4 Polyclonal Antibody

Product Specifications

Background

ADAM metallopeptidase with thrombospondin type 1 motif 4 (ADAMTS4) Homo sapiens This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Members of this family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The enzyme encoded by this gene lacks a C-terminal TS motif. The encoded preproprotein is proteolytically processed to generate the mature protease. This protease is responsible for the degradation of aggrecan, a major proteoglycan of cartilage, and brevican, a brain-specific extracellular matrix protein. The expression of this gene is upregulated in arthritic disease and this may contribute to disease progression through the degradatio

Gene ID

9507

Swiss Prot

O75173

Cross Reactivity

Human; Mouse; Rat

Clonality

Polyclonal

Source

Rabbit

Applications

WB; ELISA

Dilution

WB 1:500-2000 ELISA 1:5000-20000

Buffer

Liquid in PBS containing 50% glycerol, and 0.02% sodium azide.

Molecular Weight

92

Storage Conditions

-20°C/1 year

Protein Weight

92

Available Sizes

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