BSCL2 anticorps (N-Term)

N° du produit ABIN954710

Détail du produit anti-BSCL2 anticorps

Antigène: BSCL2 (Berardinelli-Seip Congenital Lipodystrophy 2 (Seipin) (BSCL2))

Épitope: AA 85-115, N-Term

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp BSCL2 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)

Specificité: This antibody reacts to Seipin.

Réactivité croisée (Details): Species reactivity (tested):Human.

Purification: Affinity chromatography on Protein A

Immunogène: KLH conjugated synthetic peptide between 85-115 amino acids from the N-terminal region of human BSCL2

Isotype: Ig Fraction

Information d'application

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

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.25 mg/mL

Buffer: PBS containing 0.09 % (W/V) sodium azide as preservative

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 freezing and thawing.

Stock: 4 °C/-20 °C

Stockage commentaire: Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.

Détails sur BSCL2

Antigène: BSCL2 (Berardinelli-Seip Congenital Lipodystrophy 2 (Seipin) (BSCL2))

Autre désignation: Seipin / BSCL2 (BSCL2 Produits)

Synonymes: anticorps GNG3LG, anticorps HMN5, anticorps SPG17, anticorps 2900097C17Rik, anticorps AI046355, anticorps Gng3lg, anticorps BSCL2, seipin lipid droplet biogenesis associated, anticorps Berardinelli-Seip congenital lipodystrophy 2 (seipin), anticorps BSCL2, anticorps Bscl2

Sujet: This gene encodes protein seipin, which is located in the endoplasmic reticulum and may be important for lipid droplet morphology. Mutations in this gene have been associated with congenital generalized lipodystrophy type 2 or Berardinelli-Seip syndrome, a rare autosomal recessive disease characterized by a near absence of adipose tissue and severe insulin resistance. Alternatively spliced transcript variants encoding different isoforms have been found for this geneSynonyms: Bernardinelli-Seip congenital lipodystrophy type 2 protein

ID gène: 26580

NCBI Accession: NP_001116427