SLC39A13 anticorps (N-Term)

N° du produit ABIN783815

Détail du produit anti-SLC39A13 anticorps

Antigène: SLC39A13 (Solute Carrier Family 39 (Zinc Transporter), Member 13 (SLC39A13))

Épitope: N-Term

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SLC39A13 est non-conjugé

Application: Western Blotting (WB), Enzyme Immunoassay (EIA)

Specificité: This antibody detects Zinc transporter ZIP13 / SLC39A13 at N-term.

Réactivité croisée (Details): Species reactivity (tested):Human

Purification: Affinity chromatography purified via peptide column

Immunogène: 14 amino acid peptide near the amino terminus of human ZIP13

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

Buffer: PBS containing 0.02 % sodium azide

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Conseil sur la manipulation: Avoid repeated freezing and thawing.

Stock: 4 °C/-20 °C

Stockage commentaire: Store at 2 - 8 °C for up to three months or (in aliquots) at -20 °C for longer.

Détails sur SLC39A13

Antigène: SLC39A13 (Solute Carrier Family 39 (Zinc Transporter), Member 13 (SLC39A13))

Autre désignation: Zinc Transporter ZIP13 / SLC39A13 (SLC39A13 Produits)

Synonymes: anticorps 1100001L14Rik, anticorps AA387663, anticorps ZIP13, anticorps solute carrier family 39 (metal ion transporter), member 13, anticorps solute carrier family 39 member 13, anticorps Slc39a13, anticorps SLC39A13

Sujet: The zinc transporter ZIP13, also known as SLC39A13, is a member of a family of divalent ion transporters. Zinc is an essential ion for cells and plays significant roles in the growth, development, and differentiation. The zinc transporter family is divided into four subfamilies (I, II, LIV-1 and gufA). ZIP13 is a multipass membrane protein that belongs to the ZIP transporter subfamily LIV-1. Mutations in ZIP13 have recently been shown to cause a spondylocheiro dysplastic form of Ehlers-Danlos syndrome (SCD-EDS), a generalized skeletal dysplasia involving mainly the spine with clinical abnormalities of the hands in addition to EDS-like features. Other experiments have shown that ZIP13 is required for proper connective tissue development and is involved in BMP/TGF- signaling pathways.Synonyms: LIV-1 subfamily of ZIP zinc transporter 9, LZT-Hs9, Solute carrier family 39 member 13, ZIP-13, ZIP13, Zrt-and Irt-like protein 13

ID gène: 91252

NCBI Accession: NP_001121697

UniProt: Q96H72

Pathways: Transition Metal Ion Homeostasis