CLPTM1 antibody (AA 75-120)

Catalog No. ABIN873161

The Rabbit Polyclonal anti-CLPTM1 antibody is suitable to detect CLPTM1 in samples from Human. It has been validated for WB, IF (p), IF (cc), IHC (fro) and IHC (p).

Quick Overview for CLPTM1 antibody (AA 75-120) (ABIN873161)

Target: CLPTM1 (Cleft Lip and Palate Associated Transmembrane Protein 1 (CLPTM1))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CLPTM1 antibody is un-conjugated

Application: Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunofluorescence (Cultured Cells) (IF (cc)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Product Details anti-CLPTM1 Antibody

Binding Specificity: AA 75-120

Purpose: CLPTM1 Polyclonal Antibody

Predicted Reactivity: Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Horse,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human CLPTM1

Isotype: IgG

Application Details

Application Notes: WB(1:300-5000),

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 4C. Store at -20C for one year. Avoid repeated freeze/thaw cycles.

Expiry Date: 12 months

Target Details for CLPTM1

Target: CLPTM1 (Cleft Lip and Palate Associated Transmembrane Protein 1 (CLPTM1))

Alternative Name: CLPTM1

Background:

Synonyms: Cleft lip and palate associated transmembrane protein 1, CLPTM 1, HS9, N14, CLPT1_HUMAN.

Background: Clefts of the oral-facial region usually occur in early fetal development and can affect the lip, the soft palate (the soft tissue in the back of the mouth) and the hard palate (the roof of the mouth). Cleft lip (with or without cleft palate) is a genetically complex birth defect that occurs in approximately one in every 750-1,000 live births. This is one of the most common birth defects and is multifactorial, with both genetic and environmental causes. Cleft lip- and palate-associated transmembrane protein 1 (CLPTM1) belongs to a family of cleft lip and palate transmembrane proteins. This family also contains cisplatin resistance-related protein (CRR9), which is involved in CDDP-induced apoptosis. The CLPTM1 protein shows strong homology to two Caenorhabditis elegans genes.

Gene ID: 1209