C16orf57 anticorps (AA 1-265)

N° du produit ABIN6149979

Détail du produit anti-C16orf57 anticorps

Antigène: C16orf57 (USB1) (U6 SnRNA Biogenesis 1 (USB1))

Épitope: AA 1-265

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C16orf57 est non-conjugé

Application: Western Blotting (WB)

Séquence: MSAAPLVGYS SSGSEDESED GMRTRPGDGS HRRGQSPLPR QRFPVPDSVL NMFPGTEEGP EDDSTKHGGR VRTFPHERGN WATHVYVPYE AKEEFLDLLD VLLPHAQTYV PRLVRMKVFH LSLSQSVVLR HHWILPFVQA LKARMTSFHR FFFTANQVKI YTNQEKTRTF IGLEVTSGHA QFLDLVSEVD RVMEEFNLTT FYQDPSFHLS LAWCVGDARL QLEGQCLQEL QAIVDGFEDA EVLLRVHTEQ VRCKSGNKFF SMPLK

Réactivité croisée: Humain, Souris

Attributs du produit: Polyclonal Antibodies

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 1-265 of human USB1 (NP_078874.2).

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

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.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur C16orf57

Antigène: C16orf57 (USB1) (U6 SnRNA Biogenesis 1 (USB1))

Autre désignation: USB1 (USB1 Produits)

Synonymes: anticorps C16orf57, anticorps HVSL1, anticorps Mpn1, anticorps PN, anticorps hUsb1, anticorps C18H16orf57, anticorps AA960436, anticorps RGD1305215, anticorps c16orf57, anticorps C2H16orf57, anticorps zgc:91896, anticorps U6 snRNA biogenesis phosphodiesterase 1, anticorps U6 snRNA biogenesis 1, anticorps U6 snRNA biogenesis phosphodiesterase 1 L homeolog, anticorps USB1, anticorps Usb1, anticorps usb1.L, anticorps usb1

Sujet: This gene encodes a protein with several conserved domains, however, its exact function is not known. Mutations in this gene are associated with poikiloderma with neutropenia (PN), which shows phenotypic overlap with Rothmund-Thomson syndrome (RTS) caused by mutations in the RECQL4 gene. It is believed that this gene product interacts with RECQL4 protein via SMAD4 proteins, explaining the partial clinical overlap between PN and RTS. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.,USB1,C16orf57,HVSL1,Mpn1,PN,hUsb1,Cell Biology & Developmental Biology,USB1

Poids moléculaire: 20 kDa/28 kDa/30 kDa

ID gène: 79650

UniProt: Q9BQ65