SLC26A4 anticorps (Middle Region)

N° du produit ABIN2776965

Détail du produit anti-SLC26A4 anticorps

Antigène: SLC26A4 (Solute Carrier Family 26, Member 4 (SLC26A4))

Épitope: Middle Region

Reactivité: Humain, Rat, Souris, Lapin, Boeuf (Vache), Chien, Cobaye, Cheval

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SLC26A4 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC)

Séquence: ELNDRFRHKI PVPIPIEVIV TIIATAISYG ANLEKNYNAG IVKSIPRGFL

Homologie: Cow: 92%, Dog: 100%, Guinea Pig: 100%, Horse: 93%, Human: 100%, Mouse: 100%, Rabbit: 100%, Rat: 92%

Attributs du produit: This is a rabbit polyclonal antibody against SLC26A4. It was validated on Western Blot using a cell lysate as a positive control.

Purification: Affinity Purified

Immunogène: The immunogen is a synthetic peptide directed towards the middle region of human SLC26A4

Information d'application

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

Commentaires:

Antigen size: 780 AA

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: Lot specific

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

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 freeze-thaw cycles.

Stock: -20 °C

Stockage commentaire: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

Détails sur SLC26A4

Antigène: SLC26A4 (Solute Carrier Family 26, Member 4 (SLC26A4))

Autre désignation: SLC26A4 (SLC26A4 Produits)

Synonymes: anticorps Pds, anticorps DFNB4, anticorps EVA, anticorps PDS, anticorps TDH2B, anticorps pendrin, anticorps solute carrier family 26 member 4, anticorps solute carrier family 26, member 4, anticorps SLC26A4, anticorps Slc26a4

Sujet: Mutations in this gene are associated with Pendred syndrome, the most common form of syndromic deafness, an autosomal-recessive disease. It is highly homologous to the SLC26A3 gene, they have similar genomic structures and this gene is located 3' of the S
Alias Symbols: DFNB4, PDS, EVA, TDH2B
Protein Size: 780

Poids moléculaire: 86 kDa

ID gène: 5172

NCBI Accession: NM_000441, NP_000432

UniProt: O43511

Pathways: Thyroid Hormone Synthesis, Sensory Perception of Sound