CRTAP anticorps (N-Term)

N° du produit ABIN5532526

Détail du produit anti-CRTAP anticorps

Antigène: CRTAP (Cartilage Associated Protein (CRTAP))

Épitope: AA 31-59, N-Term

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CRTAP est non-conjugé

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

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: This CRTAP antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 31-59 amino acids from the N-terminal region of human CRTAP.

Isotype: Ig Fraction

Information d'application

Indications d'application: For IF starting dilution is: 1:25

For WB starting dilution is: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Supplied in PBS with 0.09 % (W/V) sodium azide.

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: 4 °C,-20 °C

Stockage commentaire: Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Détails sur CRTAP

Antigène: CRTAP (Cartilage Associated Protein (CRTAP))

Autre désignation: CRTAP (CRTAP Produits)

Synonymes: anticorps zgc:85621, anticorps wu:fb47h01, anticorps CASP, anticorps LEPREL3, anticorps OI7, anticorps 5730529N23Rik, anticorps Leprel3, anticorps RGD1565180, anticorps cartilage associated protein, anticorps cartilage-associated protein, anticorps crtap, anticorps CRTAP, anticorps LOC5574430, anticorps CpipJ_CPIJ013810, anticorps Crtap

Sujet: The protein encoded by this gene is similar to the chicken and mouse CRTAP genes. The encoded protein is a scaffolding protein that may influence the activity of at least one member of the cytohesin/ARNO family in response to specific cellular stimuli. Defects in this gene are associated with osteogenesis imperfecta, a connective tissue disorder characterized by bone fragility and low bone mass.

Poids moléculaire: 47 kDa

ID gène: 10491

UniProt: O75718