FERMT1 anticorps (N-Term)

N° du produit ABIN2775442

L’anticorps Lapin Polyclonal anti-FERMT1 a été validé pour WB. Il convient pour détecter FERMT1 dans des échantillons de Humain, Rat, Boeuf (Vache), Chien, Cheval et Lapin.

Aperçu rapide pour FERMT1 anticorps (N-Term) (ABIN2775442)

Antigène: FERMT1 (Fermitin Family Member 1 (FERMT1))

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

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FERMT1 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-FERMT1 anticorps

Épitope: N-Term

Séquence: LSSTDFTFAS WELVVRVDHP NEEQQKDVTL RVSGDLHVGG VMLKLVEQIN

Homologie: Cow: 86%, Dog: 86%, Horse: 86%, Human: 100%, Rabbit: 93%, Rat: 79%

Attributs du produit: This is a rabbit polyclonal antibody against FERMT1. 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 N terminal region of human FERMT1

Information d'application

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

Commentaires:

Antigen size: 677 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 FERMT1

Antigène: FERMT1 (Fermitin Family Member 1 (FERMT1))

Autre désignation: FERMT1

Sujet: FERMT1 is involved in cell adhesion, possibly via its interaction with integrins. It may mediate TGF-beta 1 signaling in tumor progression. Defects in FERMT1 are the cause of Kindler syndrome.
Alias Symbols: C20orf42, DTGCU2, FLJ20116, FLJ23423, KIND1, URP1, unc112a, UNC112A
Protein Interaction Partner: SRPK1,
Protein Size: 677

Poids moléculaire: 77 kDa

ID gène: 55612

NCBI Accession: NM_017671, NP_060141

UniProt: Q9BQL6