UFD1L antibody

Catalog No. ABIN5698664

The Rabbit Polyclonal anti-UFD1L antibody is suitable to detect UFD1L in samples from Human, Mouse and Rat. It has been validated for WB, IHC, IF, ELISA and IP.

Quick Overview for UFD1L antibody (ABIN5698664)

Target: UFD1L (Ubiquitin Fusion Degradation Protein 1 Homolog (UFD1L))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This UFD1L antibody is un-conjugated

Application: Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF), ELISA, Immunoprecipitation (IP)

Product Details anti-UFD1L Antibody

Purpose: UFD1 antibody

Immunogen: ubiquitin fusion degradation 1 like (yeast)

Isotype: IgG

Application Details

Application Notes: WB : 1:500-1:5000,IHC:1:20-1:200,IP:1:50O-1:5000,IF:1:10-1:100

Comment:

mouse thymus tissue were subjected to SDS PAGE followed by western blot with FNab09233( UFD1L Antibody) at dilution of 1:1000

Restrictions: For Research Use only

Handling

Buffer: PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3,

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 freeze / thaw cycles.

Storage: -20 °C

Storage Comment: -20°C for 12 months

Expiry Date: 12 months

Target Details for UFD1L

Target: UFD1L (Ubiquitin Fusion Degradation Protein 1 Homolog (UFD1L))

Alternative Name: UFD1

Background:

Synonyms: Ubiquitin recognition factor in ER-associated degradation protein 1|Ubiquitin fusion degradation protein 1 (UB fusion protein 1)|UFD1|UFD1L

Background: The protein encoded by this gene forms a complex with two other proteins, nuclear protein localization-4 and valosin-containing protein, and this complex is necessary for the degradation of ubiquitinated proteins. In addition, this complex controls the disassembly of the mitotic spindle and the formation of a closed nuclear envelope after mitosis. Mutations in this gene have been associated with Catch 22 syndrome as well as cardiac and craniofacial defects. Alternative splicing results in multiple transcript variants encoding different isoforms. A related pseudogene has been identified on chromosome 18.

Molecular Weight: 20kDa

Gene ID: 7353

UniProt: Q92890