WNT8B antibody (C-Term)

Catalog No. ABIN657869

The Rabbit Polyclonal anti-WNT8B antibody is suitable to detect WNT8B in samples from Human. It has been validated for WB.

Quick Overview for WNT8B antibody (C-Term) (ABIN657869)

Target: WNT8B (Wingless-Type MMTV Integration Site Family, Member 8B (WNT8B))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This WNT8B antibody is un-conjugated

Application: Western Blotting (WB)

Clone: RB22565

Product Details anti-WNT8B Antibody

Binding Specificity: AA 323-351, C-Term

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This WNT8B antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 323-351 amino acids from the C-terminal region of human WNT8B.

Isotype: Ig Fraction

Application Details

Application Notes: WB: 1:1000

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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: 4 °C,-20 °C

Storage Comment: WNT8B Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.

Expiry Date: 6 months

Target Details for WNT8B

Target: WNT8B (Wingless-Type MMTV Integration Site Family, Member 8B (WNT8B))

Alternative Name: WNT8B

Background: The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It encodes a protein which shows 95 % , 86 % and 71 % amino acid identity to the mouse, zebrafish and Xenopus Wnt8B proteins, respectively. The expression patterns of the human and mouse genes appear identical and are restricted to the developing brain. The chromosomal location of this gene to 10q24 suggests it as a candidate gene for partial epilepsy.

Molecular Weight: 38721

Gene ID: 7479

NCBI Accession: NP_003384

UniProt: Q93098

Pathways: WNT Signaling