SCFD2 antibody (AA 20-585) (PE)

Catalog No. ABIN8034875

This Rabbit Polyclonal antibody specifically detects SCFD2 in FACS. It exhibits reactivity toward Human and Mouse.

Quick Overview for SCFD2 antibody (AA 20-585) (PE) (ABIN8034875)

Target: SCFD2 (Sec1 Family Domain Containing 2 (SCFD2))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SCFD2 antibody is conjugated to PE

Application: Flow Cytometry (FACS)

Product Details anti-SCFD2 Antibody (PE)

Binding Specificity: AA 20-585

Purpose: Anti-SCFD2 Antibody PE Conjugated

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

Purification: Immunogen affinity purified.

Immunogen: E.coli-derived human SCFD2 recombinant protein (Position: K20-H585).

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 SCFD2

Target: SCFD2 (Sec1 Family Domain Containing 2 (SCFD2))

Alternative Name: SCFD2

Background:

Background: SCFD2 (sec1 family domain containing 2), also known as STXBP1L1 (syntaxinbinding protein 1-like 1), is a 684 amino acid protein suggested to play a role in protein transport. Existing as two alternatively spliced isoforms, SCFD2 is a member of the STXBP/unc-18/SEC1 family and is encoded by a gene that maps to human chromosome 4q12. Chromosome 4 represents approximately 6 % of the human genome and contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is on chromosome 4. FGFR-3 is also encoded on chromosome 4 and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease

Gene Full Name: sec1 family domain containing 2

Gene ID: 152579

UniProt: Q8WU76