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SPTA1 antibody

The Rabbit Polyclonal anti-SPTA1 antibody has been validated for IHC and IF. It is suitable to detect SPTA1 in samples from Human, Mouse and Rat.
Catalog No. ABIN7256054

Quick Overview for SPTA1 antibody (ABIN7256054)

Target

See all SPTA1 Antibodies
SPTA1 (Spectrin alpha 1, Erythrocytic (SPTA1))

Reactivity

  • 67
  • 12
  • 4
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 39
  • 29
Rabbit

Clonality

  • 55
  • 13
Polyclonal

Conjugate

  • 29
  • 5
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This SPTA1 antibody is un-conjugated

Application

  • 50
  • 49
  • 40
  • 9
  • 6
  • 4
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein of human SPTA1 (NP_003117.2).

    Isotype

    IgG
  • Application Notes

    IHC 1:50-1:200 IF 1:50-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    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

    SPTA1 (Spectrin alpha 1, Erythrocytic (SPTA1))

    Alternative Name

    SPTA1

    Background

    Spectrin is an actin crosslinking and molecular scaffold protein that links the plasma membrane to the actin cytoskeleton, and functions in the determination of cell shape, arrangement of transmembrane proteins, and organization of organelles. It is a tetramer made up of alpha-beta dimers linked in a head-to-head arrangement. This gene is one member of a family of alpha-spectrin genes. The encoded protein is primarily composed of 22 spectrin repeats which are involved in dimer formation. It forms weaker tetramer interactions than non-erythrocytic alpha spectrin, which may increase the plasma membrane elasticity and deformability of red blood cells. Mutations in this gene result in a variety of hereditary red blood cell disorders, including elliptocytosis type 2, pyropoikilocytosis, and spherocytic hemolytic anemia.

    Gene ID

    6708

    UniProt

    P02549

    Pathways

    Regulation of Actin Filament Polymerization
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