SLC35D1 Rabbit Polyclonal Antibody

CAT#: TA306576

Rabbit Polyclonal Slc35D1 Antibody

Product Images

Western blot analysis of Slc35D1 in Daudi lysate with Slc35D1 antibody at (A) 1 and (B) 2 ug/mL.

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  Immunocytochemistry of Slc35D1 in Daudi cells with Slc35D1 antibody at 5 ug/mL.

Specifications

Product Data

• Applications: IF, WB
• Recommended Dilution: WB: 1 - 2 ug/mL, ICC: 5 ug/mL
• Reactivities: Human
• Host: Rabbit
• Isotype: IgG
• Clonality: Polyclonal
• Immunogen: Slc35D1 antibody was raised against a 20 amino acid peptide near the carboxy terminus of the human Slc35D1.
• Formulation: PBS containing 0.02% sodium azide.
• Concentration: 1ug/ul
• Purification: Affinity chromatography purified via peptide column
• Conjugation: Unconjugated
• Storage: Store at -20°C as received.
• Stability: Stable for 12 months from date of receipt.
• Gene Name: solute carrier family 35 member D1
• Database Link:
  NP_055954
  Entrez Gene 23169 Human
  UniProt ID Q9NTN3
• 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. This antibody is predicted to not cross-react with the highly homologous Slc35D2.
• Synonyms: UGTREL7

Reference Data

• Protein Families: Transmembrane