PJA1 antibody

Catalog No. ABIN7230658

This anti-PJA1 antibody is a Rabbit Polyclonal antibody detecting PJA1 in WB and ELISA. Suitable for Human.

Quick Overview for PJA1 antibody (ABIN7230658)

Target: PJA1 (Praja Ring Finger 1, E3 Ubiquitin Protein Ligase (PJA1))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PJA1 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-PJA1 Antibody

Purpose: PJA1 Polyclonal Antibody

Specificity: The antibody detects endogenous levels of PJA1 protein

Purification: The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

Immunogen: Synthesized peptide derived from part region of human PJA1 protein

Isotype: IgG

Application Details

Application Notes: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).

Comment:

Primary Antibody

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

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: -20 °C

Storage Comment: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Target Details for PJA1

Target: PJA1 (Praja Ring Finger 1, E3 Ubiquitin Protein Ligase (PJA1))

Alternative Name: PJA1

Background: Rabbit Anti-PJA1 Polyclonal Antibody,E3 ubiquitin-protein ligase Praja-1, Praja1, RING finger protein 70, RING-type E3 ubiquitin transferase Praja-1,PJA1 encodes an enzyme that has E2-dependent E3 ubiquitin-protein ligase activity. This enzyme belongs to a class of ubiquitin ligases that include a RING finger motif, and it can interact with the E2 ubiquitin-conjugating enzyme UbcH5B. This gene is located in an area of chromosome X where several X-linked cognitive disability disorders have been associated, and it has also been found as part of a contiguous gene deletion associated with craniofrontonasal syndrome, though a direct link to any disorder has yet to be demonstrated. Alternative splicing results in multiple transcript variants.,PJA1

Molecular Weight: observerd band 70kDa

Gene ID: 64219

UniProt: Q8NG27