TDGF1 antibody (AA 31-150)

Catalog No. ABIN731423

The Rabbit Polyclonal anti-TDGF1 antibody has been validated for ELISA. It is suitable to detect TDGF1 in samples from Human.

Quick Overview for TDGF1 antibody (AA 31-150) (ABIN731423)

Target: TDGF1 (Teratocarcinoma-Derived Growth Factor 1 (TDGF1))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This TDGF1 antibody is un-conjugated

Application: ELISA

Product Details anti-TDGF1 Antibody

Binding Specificity: AA 31-150

Cross-Reactivity: Human

Predicted Reactivity: Mouse,Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human Teratocarcinoma-derived growth factor 1

Isotype: IgG

Application Details

Application Notes: ELISA 1:500-1000

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Expiry Date: 12 months

Target Details for TDGF1

Target: TDGF1 (Teratocarcinoma-Derived Growth Factor 1 (TDGF1))

Alternative Name: CRIPTO

Background:

Synonyms: CRIPTO, CRIPT, CR, CRGF, Cripto 1, Cripto-1, Cripto 1 growth factor, Cripto-1 growth factor, Cripto1, Cripto1 growth factor, Epidermal growth factor like cripto protein CR1, Epidermal growth factor-like cripto protein CR1, TDGF 1, TDGF-1, TDGF1, Teratocarcinoma derived growth factor 1, Teratocarcinoma-derived growth factor 1, teratocarcinoma-derived growth factor 1 isoform 1 precursor, TDGF1_HUMAN.

Background: This gene encodes an epidermal growth factor-related protein that contains a cripto, FRL-1, and cryptic domain. The encoded protein is an extracellular, membrane-bound signaling protein that plays an essential role in embryonic development and tumor growth. Mutations in this gene are associated with forebrain defects. Pseudogenes of this gene are found on chromosomes 2, 3, 6, 8, 19 and X. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010].

Gene ID: 6997

Pathways: EGFR Signaling Pathway