SLC22A5 antibody

Catalog No. ABIN7258130

Product Details anti-SLC22A5 Antibody

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

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SLC22A5 antibody is un-conjugated

Application: Immunohistochemistry (IHC)

Characteristics: Polyclonal Antibody

Purification: Affinity purification

Immunogen: Recombinant protein of human SLC22A5

Isotype: IgG

Application Details

Application Notes: IHC 1:50-1:200

Restrictions: For Research Use only

Handling

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 Details for SLC22A5

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

Alternative Name: SLC22A5 (SLC22A5 Products)

Synonyms: CDSP antibody, OCTN2 antibody, OCTN2VT antibody, Lstpl antibody, Octn2 antibody, jvs antibody, slc22a5 antibody, MGC68932 antibody, CT1 antibody, UST2r antibody, ATOCT2 antibody, OCT2 antibody, ORGANIC CATION TRANSPORTER 2 antibody, YUP8H12R.2 antibody, YUP8H12R_2 antibody, organic cation/carnitine transporter 2 antibody, solute carrier family 22 member 5 antibody, solute carrier family 22 (organic cation transporter), member 5 antibody, solute carrier family 22 member 5 L homeolog antibody, organic cation/carnitine transporter 2 antibody, SLC22A5 antibody, Slc22a5 antibody, LOC100358417 antibody, slc22a5.L antibody, OCT2 antibody

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