DDHD1 antibody (AA 63-711) (Fluoro488)

Catalog No. ABIN7983940

The Rabbit Polyclonal anti-DDHD1 antibody is suitable to detect DDHD1 in samples from Human, Mouse and Rat. It has been validated for FACS.

Quick Overview for DDHD1 antibody (AA 63-711) (Fluoro488) (ABIN7983940)

Target: DDHD1 (DDHD Domain Containing 1 (DDHD1))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This DDHD1 antibody is conjugated to Fluoro488

Application: Flow Cytometry (FACS)

Product Details anti-DDHD1 Antibody (Fluoro488)

Binding Specificity: AA 63-711

Purpose: Anti-DDHD1 Antibody Fluoro488 Conjugated

Cross-Reactivity (Details): No cross-reactivity with other proteins

Purification: Immunogen affinity purified.

Immunogen: E.coli-derived human DDHD1 recombinant protein (Position: P63-S711).

Isotype: IgG

Application Details

Application Notes: Flow Cytometry, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 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.

Storage: -20 °C

Storage Comment: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Expiry Date: 12 months

Target Details for DDHD1

Target: DDHD1 (DDHD Domain Containing 1 (DDHD1))

Alternative Name: DDHD1

Background:

Background: This gene is a member of the intracellular phospholipase A1 gene family. The protein encoded by this gene preferentially hydrolyzes phosphatidic acid. It is a cytosolic protein with some mitochondrial localization, and is thought to be involved in the regulation of mitochondrial dynamics. Overexpression of this gene causes fragmentation of the tubular structures in mitochondria, while depletion of the gene results in mitochondrial tubule elongation. Deletion of this gene in male mice caused fertility defects, resulting from disruption in the organization of the mitochondria during spermiogenesis. In humans, mutations in this gene have been associated with hereditary spastic paraplegia (HSP), also known as Strumpell-Lorrain disease, or, familial spastic paraparesis (FSP). This inherited disorder is characterized by progressive weakness and spasticity of the legs. Alternative splicing results in multiple transcript variants encoding different isoforms.

Gene Full Name: DDHD domain containing 1

Gene ID: 80821

UniProt: Q8NEL9