FAM161A anticorps (C-Term)

N° du produit ABIN2788447

Cet anticorps Lapin Polyclonal détecte spécifiquement FAM161A dans WB. Il présente une réactivité envers Humain, Chien, Souris, Lapin, Cheval, Porc, Boeuf (Vache) et Rat.

Aperçu rapide pour FAM161A anticorps (C-Term) (ABIN2788447)

Antigène: FAM161A (Family with Sequence Similarity 161, Member A (FAM161A))

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

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FAM161A est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-FAM161A anticorps

Épitope: C-Term

Séquence: CNPPVPTVSS RGREQAVRKS EKERMREYQR ELEEREEKLK KRPLLFERVA

Homologie: Cow: 93%, Dog: 93%, Horse: 93%, Human: 100%, Mouse: 79%, Pig: 93%, Rabbit: 90%, Rat: 100%

Attributs du produit: This is a rabbit polyclonal antibody against FAM161A. It was validated on Western Blot.

Purification: Affinity Purified

Information d'application

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

Commentaires:

Antigen size: 551 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 FAM161A

Antigène: FAM161A (Family with Sequence Similarity 161, Member A (FAM161A))

Autre désignation: FAM161A

Sujet: This gene belongs to the FAM161 family. It is expressed mainly in the retina. Mouse studies suggested that this gene is involved in development of retinal progenitors during embryogenesis, and that its activity is restricted to mature photoreceptors after birth. Mutations in this gene cause autosomal recessive retinitis pigmentosa-28.
Alias Symbols: FLJ13305, MGC129982, MGC129983, RP28
Protein Interaction Partner: DHX32, NECAB2, TFIP11, MTUS2, ZBTB43, NINL, ZBTB1, MID2, EHMT2, RUNDC3A, PNMA2, IKZF1, TNIP1, CALCOCO2, TMCC2, KIAA0753, PDE4DIP, STX11, CADPS, PPFIA1, ZBTB14, TRAF1, TRIM37, MDFI, MCM6, KRTAP5-9, PHC2, CDR2, ZBTB8A, KRTAP10-3, KRTAP10-9, KRTAP10-7, CEP57
Protein Size: 551

Poids moléculaire: 65 kDa

ID gène: 84140

NCBI Accession: NM_032180, NP_115556

UniProt: Q3B820