TMEM147 antibody (AA 51-150) (AbBy Fluor® 680)

Catalog No. ABIN5011700

This anti-TMEM147 antibody is a Rabbit Polyclonal antibody detecting TMEM147 in WB, IF (cc) and IF (p). Suitable for Human.

Quick Overview for TMEM147 antibody (AA 51-150) (AbBy Fluor® 680) (ABIN5011700)

Target: TMEM147 (Transmembrane Protein 147 (TMEM147))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This TMEM147 antibody is conjugated to AbBy Fluor® 680

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

Product Details anti-TMEM147 Antibody (AbBy Fluor® 680)

Binding Specificity: AA 51-150

Predicted Reactivity: Human,Mouse,Rat,Cow,Horse,Rabbit,Zebrafish

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human TMEM147

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Handling

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.

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Storage: -20 °C

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

Expiry Date: 12 months

Target Details for TMEM147

Target: TMEM147 (Transmembrane Protein 147 (TMEM147))

Alternative Name: TMEM147

Background:

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.

Gene ID: 10430