Human Recombinant CHST15 protein, His Tag (V2LY-0526-LY3133)

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Basic Information

Expressed Host
HEK293 Cells
Protein Species
Human
Tag
His Tag
Protein Construction
This product is Human Recombinant CHST15 protein, His Tag consist of Amino Acid: 99-561 and predicts a molecular mass of 56 kDa.
Molecule Mass
56 kDa
Sequence
Amino Acid: 99-561
Species
Human

Formulations & Storage [For reference only, actual COA shall prevail!]

Purity
>97% as determined by SDS-PAGE
Endotoxin
Please contact us for more information.
Format
Lyophilized
Reconstitution
Allow the vial and reconstitution buffer to equilibrate to room temperature. Briefly centrifuge or tap down the vial to ensure that all lyophilized powder is collected at the bottom of the vial. For the reconstitution of this product, we recommend adding PBS or sterile water to achieve a final antibody concentration of 1 mg/mL. Allow the vial to reconstitute for 10-15 minutes at room temperature with gentle agitation. Avoid vigorous shaking that can cause foaming and antibody denaturation. Aliquot into volumes based on your experiment and store liquid protein at -20°C or -80°C for long time.
Buffer
Lyophilized from sterile PBS
Preservative
None
Storage
Samples are stable for up to twelve months from date of receipt at -20°C to -80°C. Store it under sterile conditions at -20°C to -80°C. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
More Infomation

Target

Full Name
Carbohydrate Sulfotransferase 15
Function
Sulfotransferase that transfers sulfate from 3'-phosphoadenosine 5'-phosphosulfate (PAPS) to the C-6 hydroxyl group of the GalNAc 4-sulfate residue of chondroitin sulfate A and forms chondroitin sulfate E containing GlcA-GalNAc(4,6-SO4) repeating units. It also transfers sulfate to a unique non-reducing terminal sequence, GalNAc(4SO4)-GlcA(2SO4)-GalNAc(6SO4), to yield a highly sulfated structure similar to the structure found in thrombomodulin chondroitin sulfate. May also act as a B-cell receptor involved in BCR ligation-mediated early activation that mediate regulatory signals key to B-cell development and/or regulation of B-cell-specific RAG expression; however such results are unclear in vivo.
Biological Process
Chondroitin sulfate biosynthetic process Source: Reactome
Hexose biosynthetic process Source: UniProtKB
Cellular Location
Golgi apparatus membrane. A small fraction may also be present at the cell surface, where it acts as a B-cell receptor.
Topology
Cytoplasmic: 1-80
Helical: 81-101
Lumenal: 102-561
PTM
Glycosylated.

Bhattacharyya, S., Feferman, L., Han, X., Xia, K., Zhang, F., Linhardt, R. J., & Tobacman, J. K. (2020). Increased CHST15 follows decline in arylsulfatase B (ARSB) and disinhibition of non-canonical WNT signaling: potential impact on epithelial and mesenchymal identity. Oncotarget, 11(24), 2327.

Matsuda, Y., Fujii, Y., Matsukawa, M., Ishiwata, T., Nishimura, M., & Arai, T. (2019). Overexpression of carbohydrate sulfotransferase 15 in pancreatic cancer stroma is associated with worse prognosis. Oncology letters, 18(4), 4100-4105.

Liu, L. C., Wang, Y. L., Lin, P. L., Zhang, X., Cheng, W. C., Liu, S. H., ... & Wang, S. C. (2019). Long noncoding RNA HOTAIR promotes invasion of breast cancer cells through chondroitin sulfotransferase CHST15. International journal of cancer, 145(9), 2478-2487.

Sato, H., Sagara, S., Nakajima, N., Akimoto, T., Suzuki, K., Yoneyama, H., ... & Yahagi, N. (2017). Prevention of esophageal stricture after endoscopic submucosal dissection using RNA-based silencing of carbohydrate sulfotransferase 15 in a porcine model. Endoscopy, 49(05), 491-497.

Kai, Y., Tomoda, K., Yoneyama, H., Kitabatake, M., Nakamura, A., Ito, T., ... & Kimura, H. (2017). Silencing of carbohydrate sulfotransferase 15 hinders murine pulmonary fibrosis development. Molecular Therapy-Nucleic Acids, 6, 163-172.

Ito, Z., Takakura, K., Suka, M., Kanai, T., Saito, R., Fujioka, S., ... & Ohkusa, T. (2017). Prognostic impact of carbohydrate sulfotransferase 15 in patients with pancreatic ductal adenocarcinoma. Oncology letters, 13(6), 4799-4805.

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For research use only. Not intended for any clinical use.

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