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NMNAT1 antibody (AA 1-150)

The Rabbit Polyclonal anti-NMNAT1 antibody has been validated for WB. It is suitable to detect NMNAT1 in samples from Human.
Catalog No. ABIN7268909

Quick Overview for NMNAT1 antibody (AA 1-150) (ABIN7268909)

Target

See all NMNAT1 Antibodies
NMNAT1 (Nicotinamide Nucleotide Adenylyltransferase 1 (NMNAT1))

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This NMNAT1 antibody is un-conjugated

Application

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Western Blotting (WB)
  • Binding Specificity

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    AA 1-150

    Purpose

    NMNAT1 Rabbit pAb

    Sequence

    MENSEKTEVV LLACGSFNPI TNMHLRLFEL AKDYMNGTGR YTVVKGIISP VGDAYKKKGL IPAYHRVIMA ELATKNSKWV EVDTWESLQK EWKETLKVLR HHQEKLEASD CDHQQNSPTL ERPGRKRKWT ETQDSSQKKS LEPKTKAVPK

    Cross-Reactivity

    Human

    Characteristics

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 1-150 of human NMNAT1 (NP_073624.2).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000

    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

    NMNAT1 (Nicotinamide Nucleotide Adenylyltransferase 1 (NMNAT1))

    Alternative Name

    NMNAT1

    Background

    This gene encodes an enzyme which catalyzes a key step in the biosynthesis of nicotinamide adenine dinucleotide (NAD). The encoded enzyme is one of several nicotinamide nucleotide adenylyltransferases, and is specifically localized to the cell nucleus. Activity of this protein leads to the activation of a nuclear deacetylase that functions in the protection of damaged neurons. Mutations in this gene have been associated with Leber congenital amaurosis 9. Alternative splicing results in multiple transcript variants. Pseudogenes of this gene are located on chromosomes 1, 3, 4, 14, and 15.,NMNAT1,LCA9,NMNAT,PNAT1,Epigenetics & Nuclear Signaling,Cancer,Signal Transduction,Endocrine & Metabolism,Neuroscience,Neurodegenerative Diseases,NMNAT1

    Molecular Weight

    31kDa

    Gene ID

    64802

    UniProt

    Q9HAN9
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