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Recommended dilution
| Application | Dilution |
|---|---|
| It is recommended that this reagent should be titrated in each testing system to obtain optimal results. | |
Product Information
31019-1-PBS targets SLC35D1 in WB, Indirect ELISA applications and shows reactivity with human, mouse, rat samples.
| Tested Reactivity | human, mouse, rat |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen |
CatNo: Ag34372 Product name: Recombinant human SLC35D1 protein Source: e coli.-derived, PET28a Tag: 6*His Domain: 89-157 aa of BC093786 Sequence: VGKALRVVKFPDLDRNVPRKTFPLPLLYFGNQITGLFSTKKLNLPMFTVLRRFSILFTMFAEGVLLKKT 相同性解析による交差性が予測される生物種 |
| Full Name | solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1 |
| Calculated molecular weight | 355 aa, 39 kDa |
| Observed molecular weight | 35-39 kDa |
| GenBank accession number | BC093786 |
| Gene Symbol | SLC35D1 |
| Gene ID (NCBI) | 23169 |
| RRID | AB_3669816 |
| Conjugate | Unconjugated |
| Form | |
| Form | Liquid |
| Purification Method | Antigen affinity Purification |
| UNIPROT ID | Q9NTN3 |
| Storage Buffer | PBS only{{ptg:BufferTemp}}7.3 |
| Storage Conditions | Store at -80°C. |
Background Information
SLC35D1 belongs to the TPT transporter family and is a nucleotide sugar transporter (NST) expressed in the endoplasmic reticulum. Loss-of-function mutations in SLC35D1 cause Schneckenbecken dysplasia, a severe skeletal dysplasia (PMID: 19508970; 35934917).