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GLUD1, Blocking Peptide

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产品名称: GLUD1, Blocking Peptide
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简单介绍

GLUD1, Blocking Peptide


GLUD1, Blocking Peptide  的详细介绍
Product Name

GLUD1, Blocking Peptide

Full Product Name

GLUD1 Peptide

Product Gene Name

GLUD1 blocking peptide

[Similar Products]
Product Synonym Gene Name
GDH; GDH1; GLUD; MGC132003[Similar Products]
Antibody/Peptide Pairs
GLUD1 peptide (MBS3232842) is used for blocking the activity of GLUD1 antibody (MBS3207877)
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
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OMIM
611470
3D Structure
ModBase 3D Structure for Q5TDP6
Form/Format
Lyophilized powder
Preparation and Storage
Add 100ul of sterile PBS. Final peptide concentration is 1 mg/ml in PBS. For longer periods of storage, store at -20 degree C. Avoid repeat freeze-thaw cycles.
Other Notes
Small volumes of GLUD1 blocking peptide vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
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Related Product Information for
GLUD1 blocking peptide
This is a synthetic peptide designed for use in combination with anti-GLUD1 antibody made

Target Description: L-glutamate dehydrogenase (EC 1.4.1.3) has a central role in nitrogen metabolism in plants and animals. Glutamate dehydrogenase is found in all organisms and catalyzes the oxidative deamination of 1-glutamate to 2-oxoglutarate. Glutamate, the main substrate of GLUD, is present in brain in concentrations higher than in other organs. In nervous tissue, GLUD appears to function in both the synthesis and the catabolism of glutamate and perhaps in ammonia detoxification.L-glutamate dehydrogenase (EC 1.4.1.3) has a central role in nitrogen metabolism in plants and animals. Glutamate dehydrogenase is found in all organisms and catalyzes the oxidative deamination of 1-glutamate to 2-oxoglutarate (Smith et al., 2001 [PubMed 11254391]). Glutamate, the main substrate of GLUD, is present in brain in concentrations higher than in other organs. In nervous tissue, GLUD appears to function in both the synthesis and the catabolism of glutamate and perhaps in ammonia detoxification (Mavrothalassitis et al., 1988 [PubMed 3368458]).[supplied by OMIM]. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications. PRIMARYREFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-51 M20867.1 1-51 52-3120 BC112946.1 16-3084
Product Categories/Family for GLUD1 blocking peptide
Peptide
Applications Tested/Suitable for GLUD1 blocking peptide
Immunohistochemistry (IHC), Western Blot (WB)
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NCBI/Uniprot data below describe general gene information for GLUD1. It may not necessarily be applicable to this product.
NCBI GI #
4885281
NCBI GeneID
2746
NCBI Accession #
NP_005262 [Other Products]
NCBI GenBank Nucleotide #
NM_005271 [Other Products]
UniProt Primary Accession #
Q5TDP6 [Other Products]
UniProt Related Accession #
P00367[Other Products]
Molecular Weight
56kDa
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NCBI Official Full Name
glutamate dehydrogenase 1, mitochondrial isoform a
NCBI Official Synonym Full Names
glutamate dehydrogenase 1
NCBI Official Symbol
GLUD1  [Similar Products]
NCBI Official Synonym Symbols
GDH; GDH1; GLUD
  [Similar Products]
NCBI Protein Information
glutamate dehydrogenase 1, mitochondrial
UniProt Protein Name
Lengsin
UniProt Synonym Protein Names
Glutamate-ammonia ligase domain-containing protein 1; Lens glutamine synthase-like
UniProt Gene Name
LGSN  [Similar Products]
UniProt Synonym Gene Names
GLULD1; LGS  [Similar Products]
UniProt Entry Name
LGSN_HUMAN
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NCBI Summary for GLUD1
This gene encodes glutamate dehydrogenase, which is a mitochondrial matrix enzyme that catalyzes the oxidative deamination of glutamate to alpha-ketoglutarate and ammonia. This enzyme has an important role in regulating amino acid-induced insulin secretion. It is allosterically activated by ADP and inhibited by GTP and ATP. Activating mutations in this gene are a common cause of congenital hyperinsulinism. Alternative splicing of this gene results in multiple transcript variants. The related glutamate dehydrogenase 2 gene on the human X-chromosome originated from this gene via retrotransposition and encodes a soluble form of glutamate dehydrogenase. Related pseudogenes have been identified on chromosomes 10, 18 and X. [provided by RefSeq, Jan 2016]
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Research Articles on GLUD1
1. GLUD1 may play an important role in osteogenic differentiation of human dental pulp stem cells
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Precautions
All of MyBioSource's Products are for scientific laboratory research purposes and are not for diagnostic, therapeutics, prophylactic or in vivo use. Through your purchase, you expressly represent and warrant to MyBioSource that you will properly test and use any Products purchased from MyBioSource in accordance with industry standards. MyBioSource and its authorized distributors reserve the right to refuse to process any order where we reasonably believe that the intended use will fall outside of our acceptable guidelines.
Disclaimer
While every efforts were made to ensure the accuracy of the information provided in this datasheet, MyBioSource will not be liable for any omissions or errors contained herein. MyBioSource reserves the right to make changes to this datasheet at any time without prior notice.

It is the responsibility of the customer to report product performance issues to MyBioSource within 30 days of receipt of the product. Please visit our Terms & Conditions page for more information.
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