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SHMT1 antibody (N-Term)

This Rabbit Polyclonal antibody specifically detects SHMT1 in WB and IHC. It exhibits reactivity toward Human.
Catalog No. ABIN2798590
$443.90
Plus shipping costs $50.00
400 μL
Shipping to: United States
Delivery in 6 to 9 Business Days

Quick Overview for SHMT1 antibody (N-Term) (ABIN2798590)

Target

See all SHMT1 Antibodies
SHMT1 (serine Hydroxymethyltransferase 1 (Soluble) (SHMT1))

Reactivity

  • 45
  • 10
  • 8
  • 5
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 39
  • 8
Rabbit

Clonality

  • 40
  • 7
Polyclonal

Conjugate

  • 28
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This SHMT1 antibody is un-conjugated

Application

  • 47
  • 19
  • 15
  • 13
  • 13
  • 9
  • 8
  • 6
  • 4
  • 3
  • 2
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)
  • Binding Specificity

    • 15
    • 8
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 19-47, N-Term

    Purpose

    Rabbit Anti-Human SHMT1 (N-term) Antibody

    Immunogen

    This SHMT1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 19-47 amino acids from the N-terminal region of human SHMT1.

    Isotype

    Ig Fraction
  • Application Notes

    Western Blot, Immunohistochemistry
    Recommended Dilutions
    WB: 1:1000, IHC: 1:10-50SHMT1 Antibody (N-term) for immunohistochemistry. Clinical relevance has not been evaluated.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.5 mg/mL

    Storage

    4 °C,-20 °C

    Storage Comment

    2-8°C (short-term), -20°C (long-term)
  • Target

    SHMT1 (serine Hydroxymethyltransferase 1 (Soluble) (SHMT1))

    Alternative Name

    SHMT1

    Background

    Target Description: This gene encodes the cellular form of serine hydroxymethyltransferase, a pyridoxal phosphate-containing enzyme that catalyzes the reversible conversion of serine and tetrahydrofolate to glycine and 5,10-methylene tetrahydrofolate. This reaction provides one carbon units for synthesis of methionine, thymidylate, and purines in the cytoplasm. This gene is located within the Smith-Magenis syndrome region on chromosome 17. Alternative splicing of this gene results in 2 transcript variants encoding 2 different isoforms. Additional transcript variants have been described, but their biological validity has not been determined.

    Gene Symbol: SHMT1

    Molecular Weight

    53083 Da

    Gene ID

    6470

    UniProt

    P34896
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