TCTN2 antibody (AA 61-160)

Catalog No. ABIN1713914

Product Details anti-TCTN2 Antibody

Target: TCTN2 (Tectonic Family Member 2 (TCTN2))

Binding Specificity: AA 61-160

Reactivity: Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This TCTN2 antibody is un-conjugated

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

Cross-Reactivity: Mouse

Predicted Reactivity: Human,Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human TCTN2

Isotype: IgG

Application Details

Application Notes: WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200
ICC 1:100-500

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 TCTN2

Target: TCTN2 (Tectonic Family Member 2 (TCTN2))

Alternative Name: TCTN2 (TCTN2 Products)

Synonyms: fb44f11 antibody, wu:fb44f11 antibody, tect2 antibody, C12orf38 antibody, MKS8 antibody, TECT2 antibody, 4432405B04Rik antibody, Tect2 antibody, tectonic family member 2 antibody, TCTN2 antibody, tctn2 antibody, Tctn2 antibody

Background:

Synonyms: C12orf38, FLJ12975, MKS8, OTTHUMP00000239215, OTTHUMP00000239216, Tctn2, TECT2, TECT2_HUMAN, Tectonic family member 2, Tectonic-2.

Background: Defects in TCTN2 are the cause of Meckel syndrome type 8 (MKS8) [MIM:613885]. A disorder characterized by a combination of renal cysts and variably associated features including developmental anomalies of the central nervous system (typically encephalocele), hepatic ductal dysplasia and cysts, and polydactyly.

Pathways: Proton Transport