GDF6 antibody (Internal Region)

Catalog No. ABIN7218798

This Rabbit Polyclonal antibody specifically detects GDF6 in WB and ELISA. It exhibits reactivity toward Human, Mouse and Rat.

Quick Overview for GDF6 antibody (Internal Region) (ABIN7218798)

Target: GDF6 (Growth Differentiation Factor 6 (GDF6))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This GDF6 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-GDF6 Antibody

Binding Specificity: Internal Region

Purpose: Rabbit Anti-GDF-6 Polyclonal Antibody

Specificity: GDF-6 Polyclonal Antibody detects endogenous levels of GDF-6 protein.

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogen: Synthesized peptide derived from the Internal region of human GDF-6

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 1:10000,Not yet tested in other applications.

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 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: 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.

Expiry Date: 12 months

Target Details for GDF6

Target: GDF6 (Growth Differentiation Factor 6 (GDF6))

Alternative Name: GDF-6

Background: GDF6, GDF16, Growth/differentiation factor 6, GDF-6, Growth/differentiation factor 16GDF6 encodes a member of the bone morphogenetic protein (BMP) family and the TGF-beta superfamily of secreted signaling molecules. It is required for normal formation of some bones and joints in the limbs, skull, and axial skeleton. Mutations in this gene result in colobomata, which are congenital abnormalities in ocular development, and in Klippel-Feil syndrome (KFS), which is a congenital disorder of spinal segmentation.

Molecular Weight: 50kD

Gene ID: 392255

UniProt: Q6KF10