Solute Carrier Family 17 (Acidic Sugar Transporter), Member 5 (SLC17A5) (AA 1-100) antibody

Catalog No. ABIN7270404

Product Details

Target: Solute Carrier Family 17 (Acidic Sugar Transporter), Member 5 (SLC17A5)

Binding Specificity: AA 1-100

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: Un-conjugated

Application: Western Blotting (WB)

Purpose: SLC17A5 Rabbit pAb

Sequence: MRSPVRDLAR NDGEESTDRT PLLPGAPRAE AAPVCCSARY NLAILAFFGF FIVYALRVNL SVALVDMVDS NTTLEDNRTS KACPEHSAPI KVHHNQTGKK

Cross-Reactivity: Human, Rat

Characteristics: Polyclonal Antibodies

Purification: Affinity purification

Immunogen: A synthetic peptide corresponding to a sequence within amino acids 1-100 of human SLC17A5 (NP_036566.1).

Isotype: IgG

Application Details

Application Notes: WB,1:200 - 1:2000

Restrictions: For Research Use only

Handling

Format: Liquid

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

Target: Solute Carrier Family 17 (Acidic Sugar Transporter), Member 5 (SLC17A5)

Alternative Name: SLC17A5 (SLC17A5 Products)

Synonyms: AST antibody, ISSD antibody, NSD antibody, SD antibody, SIALIN antibody, SIASD antibody, SLD antibody, sialin antibody, got2 antibody, zgc:66329 antibody, 4631416G20Rik antibody, 4732491M05 antibody, SP55 antibody, sb:cb809 antibody, zgc:153077 antibody, solute carrier family 17 member 5 antibody, solute carrier family 17 member 5 S homeolog antibody, glutamic-oxaloacetic transaminase 2a, mitochondrial antibody, solute carrier family 17 (anion/sugar transporter), member 5 antibody, solute carrier family 17 (acidic sugar transporter), member 5 antibody, SLC17A5 antibody, slc17a5.S antibody, got2a antibody, Slc17a5 antibody, slc17a5 antibody

Background: This gene encodes a membrane transporter that exports free sialic acids that have been cleaved off of cell surface lipids and proteins from lysosomes. Mutations in this gene cause sialic acid storage diseases, including infantile sialic acid storage disorder and and Salla disease, an adult form.,SLC17A5,AST,ISSD,NSD,SD,SIALIN,SIASD,SLD,sialin,SLC17A5

Molecular Weight: 30kDa/54kDa

Gene ID: 26503

UniProt: Q9NRA2