SLC7A9 antibody (C-Term)

Catalog No. ABIN7466232

This Rabbit Polyclonal antibody specifically detects SLC7A9 in WB. It exhibits reactivity toward Human.

Quick Overview for SLC7A9 antibody (C-Term) (ABIN7466232)

Target: SLC7A9 (Solute Carrier Family 7 (Cationic Amino Acid Transporter, Y+ System), Member 9 (SLC7A9))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SLC7A9 antibody is un-conjugated

Application: Western Blotting (WB)

Product Details anti-SLC7A9 Antibody

Binding Specificity: C-Term

Cross-Reactivity: Human

Purification: Purified by antigen-affinity chromatography.

Immunogen: Recombinant protein encompassing a sequence within the C-terminus region of human SLC7A9. The exact sequence is proprietary.

Isotype: IgG

Application Details

Application Notes: WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Comment:

Positive Control: human kidney

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1.3 mg/mL

Buffer: 1XPBS ( pH 7), 20 % Glycerol, 0.025 % ProClin 300

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Target Details for SLC7A9

Target: SLC7A9 (Solute Carrier Family 7 (Cationic Amino Acid Transporter, Y+ System), Member 9 (SLC7A9))

Alternative Name: solute carrier family 7 member 9

Background: Solute carrier family 7 member 9 , BAT1 , CSNU3,This gene encodes a protein that belongs to a family of light subunits of amino acid transporters. This protein plays a role in the high-affinity and sodium-independent transport of cystine and neutral and dibasic amino acids, and appears to function in the reabsorption of cystine in the kidney tubule. Mutations in this gene cause non-type I cystinuria, a disease that leads to cystine stones in the urinary system due to impaired transport of cystine and dibasic amino acids. Two transcript variants, which encode the same protein, have been found for this gene. [provided by RefSeq]

Molecular Weight: 53 kDa

Gene ID: 11136

UniProt: P82251