TEX261 antibody (AA 121-196)

Catalog No. ABIN1386683

The Rabbit Polyclonal anti-TEX261 antibody has been validated for ELISA, IHC (p), ICC, IF (cc), IF (p) and IHC (fro). It is suitable to detect TEX261 in samples from Human.

Quick Overview for TEX261 antibody (AA 121-196) (ABIN1386683)

Target: TEX261 (Testis Expressed 261 (TEX261))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This TEX261 antibody is un-conjugated

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

Product Details anti-TEX261 Antibody

Binding Specificity: AA 121-196

Predicted Reactivity: Human,Dog,Cow,Sheep,Pig,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human TEX261

Isotype: IgG

Application Details

Application Notes: 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 TEX261

Target: TEX261 (Testis Expressed 261 (TEX261))

Alternative Name: TEX261

Background:

Synonyms: 3110001O07Rik, AA409339, AI480706, AL033351, Protein TEX261, TEG 261, TEX261, TX261_HUMAN, UNQ1882/PRO4325.

Background: TEX261 is a 196 amino acid multi-pass membrane protein that belongs to the SVP26 family. The gene that encodes TEX261 consists of approximately 47,406 bases and maps to human chromosome 2p13.3. Consisting of 237 million bases, Chromosome 2 encodes over 1,400 genes and makes up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome, is due to mutations in the ALMS1 gene.