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AB96129

Anti-ST3Gal I antibody

3

(1 Review)

|

(6 Publications)

Rabbit Polyclonal ST3Gal I antibody. Suitable for WB, IHC-P and reacts with Human samples. Cited in 6 publications. Immunogen corresponding to Recombinant Fragment Protein within Human ST3GAL1 aa 1-200.

View Alternative Names

SIAT4, SIAT4A, ST3GAL1, Gal-NAc6S, Monosialoganglioside sialyltransferase, SIATFL, ST3Gal I, ST3GalA.1, ST3O, Sialyltransferase 4A, ST3GalI, SIAT4-A

1 Images
Western blot - Anti-ST3Gal I antibody (AB96129)
  • WB

Supplier Data

Western blot - Anti-ST3Gal I antibody (AB96129)

Samples were separated by 12% SDS-PAGE. The signal was developed with Trident ECL plus-Enhanced. Corresponding RNA expression data for the same cell lines are based on Human Protein Atlas program.

All lanes:

Western blot - Anti-ST3Gal I antibody (ab96129) at 1/500 dilution

Lane 1:

PC-3 whole cell extracts at 30 µg

Lane 2:

K562 whole cell extracts at 30 µg

Secondary

All lanes:

HRP-conjugated anti-rabbit IgG antibody

Predicted band size: 39 kDa

true

Key facts

Host species

Rabbit

Clonality

Polyclonal

Isotype

IgG

Carrier free

No

Reacts with

Human

Applications

IHC-P, WB

applications

Immunogen

Recombinant Fragment Protein within Human ST3GAL1 aa 1-200. The exact immunogen used to generate this antibody is proprietary information.

Q11201

Reactivity data

{ "title": "Reactivity Data", "filters": { "stats": ["", "Species", "Dilution Info", "Notes"], "tabs": { "all-applications": {"fullname" : "All Applications", "shortname": "All Applications"}, "WB" : {"fullname" : "Western blot", "shortname":"WB"}, "IHCP" : {"fullname" : "Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)", "shortname":"IHC-P"} }, "product-promise": { "all": "all", "testedAndGuaranteed": "tested", "guaranteed": "expected", "predicted": "predicted", "notRecommended": "not-recommended" } }, "values": { "Human": { "WB-species-checked": "testedAndGuaranteed", "WB-species-dilution-info": "1/500 - 1/3000", "WB-species-notes": "<p></p>", "IHCP-species-checked": "guaranteed", "IHCP-species-dilution-info": "1/100 - 1/1000", "IHCP-species-notes": "<p></p>" } } }

Properties and storage information

Form
Liquid
Purification technique
Affinity purification Immunogen
Storage buffer
pH: 7 Preservative: 0.025% Proclin 300 Constituents: PBS, 20% Glycerol (glycerin, glycerine), 1% BSA
Shipped at conditions
Blue Ice
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
-20°C
Aliquoting information
Upon delivery aliquot
Storage information
Avoid freeze / thaw cycle

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

ST3Gal I also known as ST3 beta-galactoside alpha-23-sialyltransferase 1 or sialyltransferase 1 is an enzyme with a molecular mass of approximately 35 kDa. This enzyme catalyzes the transfer of sialic acid from CMP-sialic acid to galactose-containing substrates specifically creating the sialyl T antigen. ST3Gal I is expressed in many tissues including the gastrointestinal tract lungs and the immune system reflecting its diverse roles in different physiological contexts.
Biological function summary

ST3Gal I participates in glycosylation processes that modify proteins and lipids influencing cell-cell interactions immune responses and protein stability. It often associates with glycosylation complexes ensuring the proper addition of sialic acid to glycoconjugates. These modifications are critical for the formation of sialyated glycoconjugates which play significant roles in cellular communication and pathogen recognition.

Pathways

ST3Gal I impacts the sialylation pathway and by extension affects glycan biosynthesis pathways. It modifies glycoproteins and glycolipids which are important in cell adhesion and signaling pathways. Within these pathways ST3Gal I shows interactions with proteins involved in these processes such as those in the selectin family which mediate leukocyte trafficking.

Altered ST3Gal I expression or activity links to certain cancers and immune disorders. Its dysregulation can lead to aberrant glycosylation patterns impacting processes like tumor metastasis and immune evasion. For instance the sialylation of mucins which influences tumor progression requires ST3Gal I. Also its interaction with other glycosyltransferases includes the regulation of immune cell surface antigens connecting it to autoimmune conditions.

Product protocols

For this product, it's our understanding that no specific protocols are required. You can visit:

Target data

A beta-galactoside alpha2-3 sialyltransferase involved in terminal sialylation of glycoproteins and glycolipids (PubMed : 31784620, PubMed : 8027041). Catalyzes the transfer of sialic acid (N-acetyl-neuraminic acid; Neu5Ac) from the nucleotide sugar donor CMP-Neu5Ac onto acceptor Galbeta-(1->3)-GalNAc-terminated glycoconjugates through an alpha2-3 linkage (PubMed : 31784620, PubMed : 8027041). Adds sialic acid to the core 1 O-glycan, Galbeta-(1->3)-GalNAc-O-Ser/Thr, which is a major structure of mucin-type O-glycans. As part of a homeostatic mechanism that regulates CD8-positive T cell numbers, sialylates core 1 O-glycans of T cell glycoproteins, SPN/CD43 and PTPRC/CD45. Prevents premature apoptosis of thymic CD8-positive T cells prior to peripheral emigration, whereas in the secondary lymphoid organs controls the survival of CD8-positive memory T cells generated following a successful immune response (By similarity). Transfers sialic acid to asialofetuin, presumably onto Galbeta-(1->3)-GalNAc-O-Ser (By similarity). Sialylates GM1a, GA1 and GD1b gangliosides to form GD1a, GM1b and GT1b, respectively (By similarity) (PubMed : 8027041).
See full target information ST3GAL1

Publications (6)

Recent publications for all applications. Explore the full list and refine your search

Cancer cell international 25:36 PubMed39920744

2025

Comprehensive analysis of α2,3-sialyltransferases as prognostic biomarkers and immunotherapy targets in kidney renal clear cell carcinoma.

Applications

Unspecified application

Species

Unspecified reactive species

Yuli Jian,Kangkang Yang,Jinjing Li,Ling Tang,Guang Zeng,Xiaoxin Sun,Xiao Yu,Abdullah Al-Danakh,Qiwei Chen,Deyong Yang,Shujing Wang

iScience 28:111758 PubMed39906564

2025

Multilevel plasticity and altered glycosylation drive aggressiveness in hypoxic and glucose-deprived bladder cancer cells.

Applications

Unspecified application

Species

Unspecified reactive species

Andreia Peixoto,Dylan Ferreira,Andreia Miranda,Marta Relvas-Santos,Rui Freitas,Tim S Veth,Andreia Brandão,Eduardo Ferreira,Paula Paulo,Marta Cardoso,Cristiana Gaiteiro,Sofia Cotton,Janine Soares,Luís Lima,Filipe Teixeira,Rita Ferreira,Carlos Palmeira,Albert J R Heck,Maria José Oliveira,André M N Silva,Lúcio Lara Santos,José Alexandre Ferreira

Molecular & cellular proteomics : MCP 23:100821 PubMed39069074

2024

ST3GAL1 Promotes Malignant Phenotypes in Intrahepatic Cholangiocarcinoma.

Applications

Unspecified application

Species

Unspecified reactive species

Fanghua Chen,Ke Gao,Yan Li,Yin Li,Yingcheng Wu,Liangqing Dong,Zijian Yang,Jieyi Shi,Kun Guo,Qiang Gao,Haojie Lu,Shu Zhang

Oncotarget 8:29013-29027 PubMed28423672

2017

α2,3-sialyltransferase type I regulates migration and peritoneal dissemination of ovarian cancer cells.

Applications

IHC, WB

Species

Unspecified reactive species, Unspecified reactive species

Kuo-Chang Wen,Pi-Lin Sung,Shie-Liang Hsieh,Yu-Ting Chou,Oscar Kuang-Sheng Lee,Cheng-Wen Wu,Peng-Hui Wang

Laboratory investigation; a journal of technical m 96:731-40 PubMed27088512

2016

Alpha-2, 3-sialyltransferases regulate the multidrug resistance of chronic myeloid leukemia through miR-4701-5p targeting ST3GAL1.

Applications

Unspecified application

Species

Unspecified reactive species

Yan Li,Shihua Luo,Weijie Dong,Xiaobo Song,Huimin Zhou,Lifen Zhao,Li Jia

BMC cancer 15:880 PubMed26552809

2015

Prognostic significance of ST3GAL-1 expression in patients with clear cell renal cell carcinoma.

Applications

Unspecified application

Species

Unspecified reactive species

Qi Bai,Li Liu,Yu Xia,Qilai Long,Jiajun Wang,Jiejie Xu,Jianming Guo
View all publications

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