SLC29A3 antibody (C-Term) (PE)

Catalog No. ABIN8040067

The PE-conjugated Rabbit Polyclonal anti-SLC29A3 antibody (ABIN8040067) specifically detects SLC29A3 in FACS. The antibody is reactive with Human samples.

Quick Overview for SLC29A3 antibody (C-Term) (PE) (ABIN8040067)

Target: SLC29A3 (Solute Carrier Family 29 Member 3 (SLC29A3))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SLC29A3 antibody is conjugated to PE

Application: Flow Cytometry (FACS)

Product Details anti-SLC29A3 Antibody (PE)

Binding Specificity: C-Term

Purpose: Anti-SLC29A3 Antibody PE Conjugated

Cross-Reactivity (Details): No cross-reactivity with other proteins

Purification: Immunogen affinity purified.

Immunogen: A synthetic peptide corresponding to a sequence at the C-terminus of human SLC29A3.

Isotype: IgG

Application Details

Application Notes: Flow Cytometry, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

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: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Expiry Date: 12 months

Target Details for SLC29A3

Target: SLC29A3 (Solute Carrier Family 29 Member 3 (SLC29A3))

Alternative Name: SLC29A3

Background:

Background: This gene encodes a nucleoside transporter. The encoded protein plays a role in cellular uptake of nucleosides, nucleobases, and their related analogs. Mutations in this gene have been associated with H syndrome, which is characterized by cutaneous hyperpigmentation and hypertrichosis, hepatosplenomegaly, heart anomalies, and hypogonadism. A related disorder, PHID (pigmented hypertrichosis with insulin-dependent diabetes mellitus), has also been associated with mutations at this locus. Alternatively spliced transcript variants have been described.

Gene Full Name: solute carrier family 29 member 3

Gene ID: 55315

UniProt: Q9BZD2