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ALAS2 antibody (AA 1-190)

This Rabbit Polyclonal antibody specifically detects ALAS2 in WB, ELISA, IF and FACS. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN7868330
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for ALAS2 antibody (AA 1-190) (ABIN7868330)

Target

See all ALAS2 Antibodies
ALAS2 (Aminolevulinate, delta-, Synthase 2 (ALAS2))

Reactivity

  • 68
  • 48
  • 43
  • 7
  • 6
  • 5
  • 4
  • 4
  • 3
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 59
  • 9
Rabbit

Clonality

  • 48
  • 20
Polyclonal

Conjugate

  • 28
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This ALAS2 antibody is un-conjugated

Application

  • 51
  • 13
  • 12
  • 10
  • 8
  • 4
  • 3
  • 2
  • 2
Western Blotting (WB), ELISA, Immunofluorescence (IF), Flow Cytometry (FACS)
  • Binding Specificity

    • 5
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-190

    Purpose

    ALAS2 Antibody / ASB / 5-aminolevulinic acid synthase 2

    Purification

    Antigen affinity purified

    Immunogen

    Recombinant human protein (amino acids M1-D190) was used as the immunogen for the ALAS2 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the ALAS2 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the ALAS2 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    ALAS2 (Aminolevulinate, delta-, Synthase 2 (ALAS2))

    Alternative Name

    ALAS2

    Background

    Delta-aminolevulinate synthase 2 also known as ALAS2 is a protein that in humans is encoded by the ALAS2 gene. The product of this gene specifies an erythroid-specific mitochondrially located enzyme. The encoded protein catalyzes the first step in the heme biosynthetic pathway. Defects in this gene cause X-linked pyridoxine-responsive sideroblastic anemia. Alternatively spliced transcript variants encoding different isoforms have been identified.

    UniProt

    P22557

    Pathways

    Transition Metal Ion Homeostasis
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