DSE Antibody, Biotin conjugated

Code CSB-PA890925LD01HU
Size US$166
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Product Details

Full Product Name
Rabbit anti-Homo sapiens (Human) DSE Polyclonal antibody
Uniprot No.
Target Names
DSE
Alternative Names
Chondroitin glucuronate 5 epimerase antibody; Chondroitin-glucuronate 5-epimerase antibody; Dermatan sulfate epimerase antibody; Dermatan-sulfate epimerase antibody; DS epimerase antibody; DSE antibody; DSE_HUMAN antibody; DSEPI antibody; OTTHUMP00000040406 antibody; SART 2 antibody; SART-2 antibody; Squamous cell carcinoma antigen recognized by T cells 2 antibody; Squamous cell carcinoma antigen recognized by T-cells 2 antibody
Raised in
Rabbit
Species Reactivity
Human
Immunogen
Recombinant Human Dermatan-sulfate epimerase protein (23-270AA)
Immunogen Species
Homo sapiens (Human)
Conjugate
Biotin
Clonality
Polyclonal
Isotype
IgG
Purification Method
>95%, Protein G purified
Concentration
It differs from different batches. Please contact us to confirm it.
Buffer
Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, PH 7.4
Form
Liquid
Tested Applications
ELISA
Protocols
Troubleshooting and FAQs
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead Time
Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.

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Target Background

Function
Converts D-glucuronic acid to L-iduronic acid (IdoUA) residues. Plays an important role in the biosynthesis of the glycosaminoglycan/mucopolysaccharide dermatan sulfate.
Gene References into Functions
  1. Study showed that DSE is frequently upregulated in human glioma tissue and cell lines and associated with a worse tumor grade and poor overall survival. Its knockdown suppresses malignant phenotypes, whereas DSE overexpression enhances glioma cell malignancy, both in vitro and in vivo. Mechanically, DSE modulates HB-EGF-induced EGFR/ErbB2 activity and downstream signaling. PMID: 29864158
  2. study identified a homozygous DSE missense mutation (c.803C>T, p.S268L) in a male child with musculocontractural type of Ehlers-Danlos syndrome; data indicate mutation affects the epimerase activity, resulting in reduced dermatan sulfate (DS) biosynthesis and an increased synthesis or an accumulation or reduced conversion of chondroitin sulfate PMID: 23704329
  3. Dermatan sulfate epimerase 1 was highly upregulated in esophagus squamous cell carcinoma PMID: 22350411
  4. Identification of the active site of DS-epimerase 1 and requirement of N-glycosylation for enzyme function. PMID: 19004833
Involvement in disease
Ehlers-Danlos syndrome, musculocontractural type 2 (EDSMC2)
Subcellular Location
Endoplasmic reticulum membrane; Multi-pass membrane protein. Golgi apparatus membrane; Multi-pass membrane protein. Cytoplasmic vesicle membrane; Multi-pass membrane protein. Microsome membrane; Multi-pass membrane protein.
Protein Families
Dermatan-sulfate isomerase family
Tissue Specificity
Ubiquitously expressed with higher expression in kidney and ovary and lower expression in brain, colon and thymus. Also expressed in renal cell carcinomas, brain tumors, and in a part of melanomas and adenocarcinomas from organs other than the breast. Exp
Database Links

HGNC: 21144

OMIM: 605942

KEGG: hsa:29940

STRING: 9606.ENSP00000332151

UniGene: Hs.458358

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7505 Fannin St., Ste 610, Room 7 (CUBIO Innovation Center), Houston, TX 77054, USA
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