USH1G anticorps (Internal Region)

N° du produit ABIN4889610

Détail du produit anti-USH1G anticorps

Antigène: USH1G (Usher Syndrome 1G (Autosomal Recessive) (USH1G))

Épitope: Internal Region

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp USH1G est non-conjugé

Application: ELISA, Western Blotting (WB), Immunocytochemistry (ICC), Immunofluorescence (IF)

Specificité: Reacts with human and mouse USH1G

Purification: Purified (protein A)

Immunogène: Synthetic peptide of derived from internal part of human USH1G.

Information d'application

Indications d'application:

Working dilution: Optimal dilutions should be determined by the end user.
The following are guidelines only:
- WB : 1/500 to 1/2000 - ICC, IF: 1/200 to 1/1000

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Must be reconstituted in distilled water.

Concentration: 1 mg/mL

Buffer: Tris 0,1M, glycine 0,1M

Stock: 4 °C/-20 °C

Stockage commentaire: Short term storage at+4°C. For extended periods store in aliquots at -20°C. Antibodies are guaranteed for 6 month from date of receipt.

Date de péremption: 6 months

Détails sur USH1G

Antigène: USH1G (Usher Syndrome 1G (Autosomal Recessive) (USH1G))

Autre désignation: USH1G (USH1G Produits)

Synonymes: anticorps ANKS4A, anticorps SANS, anticorps Sans, anticorps js, anticorps USH1 protein network component sans, anticorps USH1G, anticorps Ush1g

Sujet: Required for normal development and maintenance of cochlear hair cell bundles. Anchoring/scaffolding protein that is a part of the functional network formed by USH1C, USH1G, CDH23 and MYO7A that mediates mechanotransduction in cochlear hair cells. Required for normal hearing.

ID gène: 124590

UniProt: Q495M9

Pathways: Sensory Perception of Sound