WHSC1 anticorps (AA 1-240)

N° du produit ABIN6150213

Cet anticorps Lapin Polyclonal détecte spécifiquement WHSC1 dans WB et IHC. Il présente une réactivité envers Humain.

Aperçu rapide pour WHSC1 anticorps (AA 1-240) (ABIN6150213)

Antigène: WHSC1 (Wolf-Hirschhorn Syndrome Candidate 1 (WHSC1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp WHSC1 est non-conjugé

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

Détail du produit anti-WHSC1 anticorps

Épitope: AA 1-240

Séquence: MEFSIKQSPL SVQSVVKCIK MKQAPEILGS ANGKTPSCEV NRECSVFLSK AQLSSSLQEG VMQKFNGHDA LPFIPADKLK DLTSRVFNGE PGAHDAKLRF ESQEMKGIGT PPNTTPIKNG SPEIKLKITK TYMNGKPLFE SSICGDSAAD VSQSEENGQK PENKARRNRK RSIKYDSLLE QGLVEAALVS KISSPSDKKI PAKKESCPNT GRDKDHLLKY NVGDLVWSKV SGYPWWPCMV

Réactivité croisée: Humain, Souris

Attributs du produit: Polyclonal Antibodies

Purification: Affinity purification

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 1-240 of human WHSC1 (NP_579877.1).

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000,IHC,1:50 - 1:200

Commentaires:

HIGH QUALITY

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 WHSC1

Antigène: WHSC1 (Wolf-Hirschhorn Syndrome Candidate 1 (WHSC1))

Autre désignation: NSD2

Sujet: This gene encodes a protein that contains four domains present in other developmental proteins: a PWWP domain, an HMG box, a SET domain, and a PHD-type zinc finger. It is expressed ubiquitously in early development. Wolf-Hirschhorn syndrome (WHS) is a malformation syndrome associated with a hemizygous deletion of the distal short arm of chromosome 4. This gene maps to the 165 kb WHS critical region and has also been involved in the chromosomal translocation t(4,14)(p16.3,q32.3) in multiple myelomas. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. Some transcript variants are nonsense-mediated mRNA (NMD) decay candidates, hence not represented as reference sequences.,NSD2,KMT3F,KMT3G,MMSET,REIIBP,TRX5,WHS,WHSC1,Epigenetics & Nuclear Signaling,Chromatin Modifying Enzymes,Methylation,Transcription Factors,NSD2

Poids moléculaire: 30 kDa/53 kDa/66 kDa/69 kDa/71 kDa/80 kDa/152 kDa

ID gène: 7468

UniProt: O96028

Pathways: SARS-CoV-2 Protein Interactome