DYNAP antibody (N-Term)

Catalog No. ABIN1539422

The Rabbit Polyclonal anti-DYNAP antibody has been validated for WB. It is suitable to detect DYNAP in samples from Human.

Quick Overview for DYNAP antibody (N-Term) (ABIN1539422)

Target: DYNAP (Dynactin Associated Protein (DYNAP))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This DYNAP antibody is un-conjugated

Application: Western Blotting (WB)

Clone: RB35932

Product Details anti-DYNAP Antibody

Binding Specificity: AA 6-34, N-Term

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

Immunogen: This C18orf26 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 6-34 amino acids from the N-terminal region of human C18orf26.

Isotype: Ig Fraction

Application Details

Application Notes: WB: 1:1000

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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.

Storage: 4 °C,-20 °C

Storage Comment: C18orf26 Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Expiry Date: 6 months

Target Details for DYNAP

Target: DYNAP (Dynactin Associated Protein (DYNAP))

Alternative Name: C18orf26

Background: C18orf26 (chromosome 18 open reading frame 26) is a 210 amino acid single pass membrane protein that is encoded by a gene which maps to human chromosome 18. Chromosome 18 houses over 300 protein-coding genes and contains nearly 76 million nucleotide bases. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas.

Gene ID: 284254

NCBI Accession: NP_775900

UniProt: Q8N1N2