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SLC22A5 antibody

The Rabbit Polyclonal anti-SLC22A5 antibody has been validated for IF. It is suitable to detect SLC22A5 in samples from Human, Rat and Mouse.
Catalog No. ABIN7009509

Quick Overview for SLC22A5 antibody (ABIN7009509)

Target

See all SLC22A5 Antibodies
SLC22A5 (Solute Carrier Family 22 Member 5 (SLC22A5))

Reactivity

  • 26
  • 16
  • 13
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
Human, Rat, Mouse

Host

  • 27
Rabbit

Clonality

  • 27
Polyclonal

Conjugate

  • 17
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This SLC22A5 antibody is un-conjugated

Application

  • 16
  • 12
  • 5
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Immunofluorescence (IF)
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein of human SLC22A5 (NP_003051.1).

    Isotype

    IgG
  • Application Notes

    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

    SLC22A5 (Solute Carrier Family 22 Member 5 (SLC22A5))

    Alternative Name

    SLC22A5

    Background

    Polyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. The encoded protein is a plasma integral membrane protein which functions both as an organic cation transporter and as a sodium-dependent high affinity carnitine transporter. The encoded protein is involved in the active cellular uptake of carnitine. Mutations in this gene are the cause of systemic primary carnitine deficiency (CDSP), an autosomal recessive disorder manifested early in life by hypoketotic hypoglycemia and acute metabolic decompensation, and later in life by skeletal myopathy or cardiomyopathy. Alternative splicing of this gene results in multiple transcript variants.

    Gene ID

    6584

    UniProt

    O76082
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