MFAP1 antibody (AA 83-437) (APC)

Catalog No. ABIN8009954

This Rabbit Polyclonal antibody specifically detects MFAP1 in FACS. It exhibits reactivity toward Human and Mouse.

Quick Overview for MFAP1 antibody (AA 83-437) (APC) (ABIN8009954)

Target: MFAP1 (Microfibrillar Associated Protein 1 (MFAP1))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This MFAP1 antibody is conjugated to APC

Application: Flow Cytometry (FACS)

Product Details anti-MFAP1 Antibody (APC)

Binding Specificity: AA 83-437

Purpose: Anti-MFAP1 Antibody APC Conjugated

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

Purification: Immunogen affinity purified.

Immunogen: E.coli-derived human MFAP1 recombinant protein (Position: D83-K437).

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 MFAP1

Target: MFAP1 (Microfibrillar Associated Protein 1 (MFAP1))

Alternative Name: MFAP1

Background:

Background: Microfibrillar-associated protein 1 is a protein that in humans is encoded by the MFAP1 gene. Microfibrils are an important component of the extracellular matrix of many tissues and can either associate with or without elastin. Several microfibril associated proteins (MFAPs) have been cloned, including MFAP1, MFAP3 and MFAP4. The MFAP1 and MFAP3 genes are localized near the fibrillin genes FBN1 and FBN2, respectively. Mutations in FBN1 are linked to Marfan syndrome. Mutations in FBN2 have been linked to congenital contractural arachnodactyly. This suggests roles for MFAP1 and MFAP3 in heritable diseases affecting microfibrils. Deletion of MFAP4 was found in 30 of 31 patients with Smith-Magenis syndrome (SMS), a clinically recognizable multiple congenital anomaly/mental retardation syndrome

Gene Full Name: microfibril associated protein 1

Gene ID: 4236

UniProt: P55081