TMEM147 anticorps (AA 51-150) (Alexa Fluor 488)

N° du produit ABIN1398490

Détail du produit anti-TMEM147 anticorps (Alexa Fluor 488)

Antigène: TMEM147 (Transmembrane Protein 147 (TMEM147))

Épitope: AA 51-150

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp TMEM147 est conjugé à/à la Alexa Fluor 488

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Homologie: Human,Mouse,Rat,Cow,Horse,Rabbit,Zebrafish

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human TMEM147

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur TMEM147

Antigène: TMEM147 (Transmembrane Protein 147 (TMEM147))

Autre désignation: TMEM147 (TMEM147 Produits)

Synonymes: anticorps 2010004E11Rik, anticorps 5033425B17Rik, anticorps Nifie14, anticorps RGD1304706, anticorps NIFIE14, anticorps nifie14, anticorps zgc:92863, anticorps Transmembrane protein 147, anticorps transmembrane protein 147, anticorps transmembrane protein 147 S homeolog, anticorps tm147, anticorps tmem147, anticorps Tmem147, anticorps TMEM147, anticorps tmem147.S

Sujet:

Synonyms: ransmembrane protein 147, Full=Protein NIE 14, TM147_HUMAN.

Background: TMEM147, also known as , NIFIE 14, is a 224 amino acid protein encoded by a gene mapping to human chromosome 19. Consisting of around 63 million bases with over 1,400 genes, chromosome 19 makes up over 2 % of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fc?receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.

ID gène: 10430