NSDHL anticorps (AA 1-240)

N° du produit ABIN7268794

Détail du produit anti-NSDHL anticorps

Antigène: NSDHL (NAD(P) Dependent Steroid Dehydrogenase-Like (NSDHL))

Épitope: AA 1-240

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp NSDHL est non-conjugé

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

Fonction: [KO Validated] NSDHL Rabbit pAb

Séquence: MEPAVSEPMR DQVARTHLTE DTPKVNADIE KVNQNQAKRC TVIGGSGFLG QHMVEQLLAR GYAVNVFDIQ QGFDNPQVRF FLGDLCSRQD LYPALKGVNT VFHCASPPPS SNNKELFYRV NYIGTKNVIE TCKEAGVQKL ILTSSASVIF EGVDIKNGTE DLPYAMKPID YYTETKILQE RAVLGANDPE KNFLTTAIRP HGIFGPRDPQ LVPILIEAAR NGKMKFVIGN GKNLVDFTFV

Réactivité croisée: Humain, Souris, Rat

Attributs du produit: Polyclonal Antibodies

Purification: Affinity purification

Classe de qualité: KO Validated

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 1-240 of human NSDHL (NP_057006.1).

Isotype: IgG

Information d'application

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

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 NSDHL

Antigène: NSDHL (NAD(P) Dependent Steroid Dehydrogenase-Like (NSDHL))

Autre désignation: NSDHL (NSDHL Produits)

Synonymes: anticorps zgc:112474, anticorps H105E3, anticorps SDR31E1, anticorps XAP104, anticorps AI747449, anticorps Bpa, anticorps Str, anticorps NAD(P) dependent steroid dehydrogenase-like, anticorps NAD(P) dependent steroid dehydrogenase-like L homeolog, anticorps NSDHL, anticorps nsdhl, anticorps nsdhl.L, anticorps Nsdhl

Sujet: The protein encoded by this gene is localized in the endoplasmic reticulum and is involved in cholesterol biosynthesis. Mutations in this gene are associated with CHILD syndrome, which is a X-linked dominant disorder of lipid metabolism with disturbed cholesterol biosynthesis, and typically lethal in males. Alternatively spliced transcript variants with differing 5' UTR have been found for this gene.,NSDHL,H105E3,SDR31E1,XAP104,Cancer,Signal Transduction,Endocrine & Metabolism,Lipid Metabolism,Cholesterol Metabolism,Cardiovascular,Lipids,NSDHL

Poids moléculaire: 41kDa

ID gène: 50814

UniProt: Q15738