SLC29A3 Antikörper (N-Term)

Produktnummer ABIN656792

Produktdetails anti-SLC29A3 Antikörper

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

Bindungsspezifität: AA 21-50, N-Term

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SLC29A3 Antikörper ist unkonjugiert

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

Aufreinigung: 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.

Klon: RB32652

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: WB: 1:1000. IHC-P: 1:10~50

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: 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.

Haltbarkeit: 6 months

Details zu SLC29A3

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

Andere Bezeichnung: SLC29A3 (SLC29A3 Produkte)

Synonyme: ENT3 antikoerper, HCLAP antikoerper, HJCD antikoerper, PHID antikoerper, Ent3 antikoerper, 4933435C21Rik antikoerper, AW987637 antikoerper, solute carrier family 29 member 3 antikoerper, solute carrier family 29 (nucleoside transporters), member 3 antikoerper, SLC29A3 antikoerper, Slc29a3 antikoerper

Hintergrund: 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.

Molekulargewicht: 51815

Gen-ID: 55315

NCBI Accession: NP_001167569, NP_060814

UniProt: Q9BZD2