C16orf57 antibody (N-Term)

Catalog No. ABIN5517969

This Rabbit Polyclonal antibody specifically detects C16orf57 in WB. It exhibits reactivity toward Human.

Quick Overview for C16orf57 antibody (N-Term) (ABIN5517969)

Target: C16orf57 (USB1) (U6 SnRNA Biogenesis 1 (USB1))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C16orf57 antibody is un-conjugated

Application: Western Blotting (WB)

Product Details anti-C16orf57 Antibody

Binding Specificity: N-Term

Purpose: USB1 Antibody - N-terminal region

Sequence: LVGYSSSGSE DESEDGMRTR PGDGSHRRGQ SPLPRQRFPV PDSVLNMFPG

Purification: Affinity purified

Immunogen: The immunogen is a synthetic peptide directed towards the N terminal region of human C16ORF57

Application Details

Application Notes: Optimal working dilution should be determined by the investigator.

Comment:

We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP80076-100UG

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.5 mg/mL

Buffer: Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

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: prevent freeze-thaw cycles

Storage: 4 °C,-20 °C

Storage Comment: For short term use, store at 2-8C up to 1 week. For long term storage, store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Target Details for C16orf57

Target: C16orf57 (USB1) (U6 SnRNA Biogenesis 1 (USB1))

Alternative Name: USB1

Background:

Background Information: This gene encodes a protein with several conserved domains, however, its exact function is not known. Mutations in this gene are associated with poikiloderma with neutropenia (PN), which shows phenotypic overlap with Rothmund-Thomson syndrome (RTS) caused by mutations in the RECQL4 gene. It is believed that this gene product interacts with RECQL4 protein via SMAD4 proteins, explaining the partial clinical overlap between PN and RTS. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.

Gene Name: U6 snRNA biogenesis phosphodiesterase 1

Alternative Symbols: PN, Mpn1, HVSL1, hUsb1, C16orf57

Protein Name: U6 snRNA phosphodiesterase

Molecular Weight: 20 kDa

Gene ID: 79650

NCBI Accession: NP_001182231

UniProt: Q9BQ65