SLC29A3 antibody (N-Term)

Catalog No. ABIN656792

The Rabbit Polyclonal anti-SLC29A3 antibody has been validated for WB and IHC (p). It is suitable to detect SLC29A3 in samples from Human.

Quick Overview for SLC29A3 antibody (N-Term) (ABIN656792)

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

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SLC29A3 antibody is un-conjugated

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone: RB32652

Product Details anti-SLC29A3 Antibody

Binding Specificity: AA 21-50, N-Term

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This SLC29A3 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 21-50 amino acids from the N-terminal region of human SLC29A3.

Isotype: Ig Fraction

Application Details

Application Notes: WB: 1:1000. IHC-P: 1:10~50

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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: 4 °C,-20 °C

Storage Comment: SLC29A3 Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.

Expiry Date: 6 months

Target Details for SLC29A3

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

Alternative Name: SLC29A3

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.

Molecular Weight: 51815

Gene ID: 55315

NCBI Accession: NP_001167569, NP_060814

UniProt: Q9BZD2