1-832-868-1888
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Catalog Number: |
24703 |
other_names: | Solute carrier family 35 member D1, UDP-glucuronic acid, UDP-N-acetylgalactosamine transporter |
Amount: |
100μg |
calculated_mw: | |
host_species: | Rabbit |
Price: |
$319 |
Swiss-Prot No: |
Swiss-Prot:Q9NTN3 |
Form of Antibody: |
Supplied in PBS containing 0.02% sodium azide. |
Storage/Stability: |
|
Immunogen: |
Raised against a 14 amino acid peptide near the amino terminus of the human Slc35D1. |
Purification: |
Affinity chromatography purified via peptide column |
Specificity/Sensitivity: |
This antibody is predicted to not cross-react with the highly homologous Slc35D2. |
Applications: |
ELISA WB |
Background: |
The solute carrier family Slc35 consists of at least 17 proteins that act as nucleotide sugar transporters localized to the Golgi apparatus and endoplasmic reticulum. The role of the ER-resident Slc family member Slc35D1 is to transport both UDP-glucuronic acid and UDP-N-acetylgalactosamine. These molecules can serve as substrates for chondroitin sulfate biosynthesis and mice lacking the Slc35D1 gene developed a lethal form of skeletal dysplasia with severe shortening of limbs and facial structures. Examination of epiphyseal cartilage in these mice revealed a decreased proliferating zone with round chrondrocytes, scarce matrices, and reduced proteoglycan aggregates. Loss of function mutations in human Slc35D1 cause Schneckenbecken dysplasia, a severe skeletal dysplasia. |
References: |
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appl_detail: |
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