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Recombinant SPR antibody

The Rabbit Monoclonal anti-SPR antibody is suitable to detect SPR in samples from Human. It has been validated for WB and IHC.
Catalog No. ABIN7828553
$394.68
Plus shipping costs $50.00
50 μL
Shipping to: United States
Delivery in 11 to 14 Business Days

Quick Overview for Recombinant SPR antibody (ABIN7828553)

Target

See all SPR Antibodies
SPR (Sepiapterin Reductase (SPR))

Antibody Type

Recombinant Antibody

Reactivity

  • 55
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Human

Host

  • 44
  • 12
Rabbit

Clonality

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Monoclonal

Conjugate

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  • 1
  • 1
  • 1
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This SPR antibody is un-conjugated

Application

  • 49
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Western Blotting (WB), Immunohistochemistry (IHC)

Clone

A748
  • Purpose

    Recombinant SPR Monoclonal Antibody

    Purification

    Protein A purified

    Isotype

    IgG, kappa
  • Application Notes

    WB 1:1000,IHC 1:100

    Restrictions

    For Research Use only
  • Concentration

    1 mg/mL

    Buffer

    PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 % protein protectant.

    Preservative

    ProClin

    Precaution of Use

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

    Storage

    -20 °C

    Storage Comment

    Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.

    Expiry Date

    12 months
  • Target

    SPR (Sepiapterin Reductase (SPR))

    Alternative Name

    SPR

    Background

    SDR38C,member,OTTHUMP,SPR,SDR38C1,8 dihydrobiopterin:NADP+ oxidoreductase),member 1,OTTHUMP00000160199,Sepiapterin reductase,Sepiapterin reductase (7,Short chain dehydrogenase/reductase family 38C,SPRE,SPR can catalyze the final one or two reductions in tetra-hydrobiopterin biosynthesis to form 5,6,7,8-tetrahydrobiopterin.Defects in SPR are the cause of dystonia DOPA-responsive due to sepiapterin reductase deficiency (DRDSPRD). In the majority of cases, patients manifest progressive psychomotor retardation, dystonia and spasticity. Cognitive anomalies are also often present. The disease is due to severe dopamine and serotonin deficiencies in the central nervous system caused by a defect in BH4 synthesis. Cat.No. Product Name Clone No. IF:{{item.impact}} Journal:{{item.journal}} ({{item.year}}) DOI:{{item.doi}} Reactivity:{{item.species}} Sample Type:{{item.sample_type}} Previous {{ page }} Next Q{{(FAQpage.currentPage - 1)*pageSize+index+1}}:{{item.name}} Previous {{ page }} Next [

    Molecular Weight

    Calculated MW: 28 kDa

    Observed MW: 27 kDa The actual band is not consistent with the expectation.

    UniProt

    P35270

    Pathways

    Regulation of Systemic Arterial Blood Pressure by Hormones, Feeding Behaviour, Smooth Muscle Cell Migration
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