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GLUD1 antibody (AA 54-240)

The Rabbit Polyclonal anti-GLUD1 antibody has been validated for WB, IHC, IP and IF. It is suitable to detect GLUD1 in samples from Human.
Catalog No. ABIN6141157
$355.00
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Quick Overview for GLUD1 antibody (AA 54-240) (ABIN6141157)

Target

See all GLUD1 Antibodies
GLUD1 (Glutamate Dehydrogenase 1 (GLUD1))

Reactivity

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  • 27
  • 25
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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This GLUD1 antibody is un-conjugated

Application

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Western Blotting (WB), Immunohistochemistry (IHC), Immunoprecipitation (IP), Immunofluorescence (IF)
  • Binding Specificity

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    AA 54-240

    Sequence

    SEAVADREDD PNFFKMVEGF FDRGASIVED KLVEDLRTRE SEEQKRNRVR GILRIIKPCN HVLSLSFPIR RDDGSWEVIE GYRAQHSQHR TPCKGGIRYS TDVSVDEVKA LASLMTYKCA VVDVPFGGAK AGVKINPKNY TDNELEKITR RFTMELAKKG FIGPGIDVPA PDMSTGEREM SWIADTY

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 54-240 of human GLUD1 (NP_005262.1).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000,IHC,1:100 - 1:200,IF,1:50 - 1:200,IP,1:50 - 1:200

    Comment

    HIGH QUALITY

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    GLUD1 (Glutamate Dehydrogenase 1 (GLUD1))

    Alternative Name

    GLUD1

    Background

    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.,GLUD1,GDH,GDH1,GLUD,Cancer,Signal Transduction,Cell Biology & Developmental Biology,Endocrine & Metabolism,Amino acid metabolism,GLUD1

    Molecular Weight

    42 kDa/46 kDa/61 kDa

    Gene ID

    2746

    UniProt

    P00367

    Pathways

    Positive Regulation of Peptide Hormone Secretion, Warburg Effect
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