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ImmunohistochemistryAntibody data
- Antibody Data
- Antigen structure
- References [4]
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- Validations [0]
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- Product number
- HPA016004 - Provider product page
- Provider
- Atlas Antibodies
- Proper citation
- Atlas Antibodies Cat#HPA016004, RRID:AB_1846731
- Product name
- Anti-CHST8
- Antibody type
- Polyclonal
- Description
- Polyclonal Antibody against Human CHST8, Gene description: carbohydrate (N-acetylgalactosamine 4-0) sulfotransferase 8, Alternative Gene Names: GALNAC-4-ST1, Validated applications: IHC, Uniprot ID: Q9H2A9, Storage: Store at +4°C for short term storage. Long time storage is recommended at -20°C.
- Reactivity
- Human
- Host
- Rabbit
- Conjugate
- Unconjugated
- Isotype
- IgG
- Vial size
- 100 µl
- Concentration
- 0.2 mg/ml
- Storage
- Store at +4°C for short term storage. Long time storage is recommended at -20°C.
- Handling
- The antibody solution should be gently mixed before use.
Submitted references Transcriptomic Landscape of von Economo Neurons in Human Anterior Cingulate Cortex Revealed by Microdissected-Cell RNA Sequencing.
The glycan-specific sulfotransferase (R77W)GalNAc-4-ST1 putatively responsible for peeling skin syndrome has normal properties consistent with a simple sequence polymorphisim
Profiling post-centrifugation delay of serum and plasma with antibody bead arrays
Whole-exome sequencing in a single proband reveals a mutation in the CHST8 gene in autosomal recessive peeling skin syndrome
Yang L, Yang Y, Yuan J, Sun Y, Dai J, Su B
Cerebral cortex (New York, N.Y. : 1991) 2019 Feb 1;29(2):838-851
Cerebral cortex (New York, N.Y. : 1991) 2019 Feb 1;29(2):838-851
The glycan-specific sulfotransferase (R77W)GalNAc-4-ST1 putatively responsible for peeling skin syndrome has normal properties consistent with a simple sequence polymorphisim
Fiete D, Mi Y, Beranek M, Baenziger N, Baenziger J
Glycobiology 2017;27(5):450-456
Glycobiology 2017;27(5):450-456
Profiling post-centrifugation delay of serum and plasma with antibody bead arrays
Qundos U, Hong M, Tybring G, Divers M, Odeberg J, Uhlen M, Nilsson P, Schwenk J
Journal of Proteomics 2013;95
Journal of Proteomics 2013;95
Whole-exome sequencing in a single proband reveals a mutation in the CHST8 gene in autosomal recessive peeling skin syndrome
Cabral R, Kurban M, Wajid M, Shimomura Y, Petukhova L, Christiano A
Genomics 2012;99(4):202-208
Genomics 2012;99(4):202-208
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