TMEM184B antibody (C-Term)

Catalog No. ABIN500976

This anti-TMEM184B antibody is a Rabbit Polyclonal antibody detecting TMEM184B in WB, IF, IHC (p) and EIA. Suitable for Human, Mouse and Rat.

Quick Overview for TMEM184B antibody (C-Term) (ABIN500976)

Target: TMEM184B (Transmembrane Protein 184B (TMEM184B))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This TMEM184B antibody is un-conjugated

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

Product Details anti-TMEM184B Antibody

Binding Specificity: C-Term

Specificity: This antibody detects TMEM184B near C-term.

Purification: Peptide affinity chromatography

Immunogen: TMEM184B antibody was raised against a 15 amino acid peptide near the carboxy terminus of human TMEM184B.

Isotype: IgG

Application Details

Application Notes: ELISA. Western blot.
Other applications not tested.
Optimal dilutions are dependent on conditions and should be determined by the user.

Restrictions: For Research Use only

Handling

Concentration: 1.0 mg/mL

Buffer: PBS containing 0.02 % sodium azide

Preservative: Sodium azide

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

Handling Advice: Avoid repeated freezing and thawing.

Storage: 4 °C/-20 °C

Storage Comment: Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.

Target Details for TMEM184B

Target: TMEM184B (Transmembrane Protein 184B (TMEM184B))

Alternative Name: TMEM184B

Background: TMEM184B, also known as C22orf5, is a 407 amino acid multi-pass membrane protein and represents a novel gene in the activation of the MAPK signaling pathway. The gene encoding TMEM184B maps to human chromosome 22, mutations in several of the genes in chromosome 22 are involved in the development of autism, schizophrenia, Phelan-McDermid syndrome and Neurofibromatosis type 2, suggesting that TMEM184B may play a role in these syndromes.Synonyms: C22orf5, Putative MAPK-activating protein FM08, Transmembrane protein 184B

Gene ID: 25829

NCBI Accession: NP_036396