TGDS Antibody

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Code CSB-PA023444LA01HU
Size US$166
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  • Immunohistochemistry of paraffin-embedded human liver cancer using CSB-PA023444LA01HU at dilution of 1:100
  • Immunohistochemistry of paraffin-embedded human glioma using CSB-PA023444LA01HU at dilution of 1:100
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Product Details

Full Product Name
Rabbit anti-Homo sapiens (Human) TGDS Polyclonal antibody
Uniprot No.
Target Names
TGDS
Alternative Names
6-dehydratase antibody; dTDP D glucose 4,6 dehydratase antibody; dTDP-D-glucose 4 antibody; Growth inhibiting protein 21 antibody; SDR2E1 antibody; TDP glucose 4,6 dehydratase antibody; TDPGD antibody; TGDS antibody; TGDS_HUMAN antibody
Raised in
Rabbit
Species Reactivity
Human
Immunogen
Recombinant Human dTDP-D-glucose 4,6-dehydratase protein (143-305AA)
Immunogen Species
Homo sapiens (Human)
Conjugate
Non-conjugated

The TGDS Antibody (Product code: CSB-PA023444LA01HU) is Non-conjugated. For TGDS Antibody with conjugates, please check the following table.

Available Conjugates
Conjugate Product Code Product Name Application
HRP CSB-PA023444LB01HU TGDS Antibody, HRP conjugated ELISA
FITC CSB-PA023444LC01HU TGDS Antibody, FITC conjugated
Biotin CSB-PA023444LD01HU TGDS Antibody, Biotin conjugated ELISA
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, IF, IHC
Recommended Dilution
Application Recommended Dilution
IF 1:25-1:100
IHC 1:20-1:200
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.

Customer Reviews and Q&A

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Target Background

Gene References into Functions
  1. Our findings widen the phenotype spectrum caused by TGDS mutations and underline the phenotypic overlap with Temtamy preaxial brachydactyly syndrome. This improves our understanding of the prenatal development and the pathogenetic mechanism of Catel-Manzke syndrome. PMID: 28422407
  2. By using haplotype reconstruction we showed that the mutation c.298G>T is probably a founder mutation. Due to the spectrum of the amino acid changes, we suggest that loss of function in TGDS is the underlying mechanism of Catel-Manzke syndrome. PMID: 25480037
Involvement in disease
Catel-Manzke syndrome (CATMANS)
Protein Families
NAD(P)-dependent epimerase/dehydratase family, dTDP-glucose dehydratase subfamily
Database Links

HGNC: 20324

OMIM: 616145

KEGG: hsa:23483

STRING: 9606.ENSP00000261296

UniGene: Hs.12393

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