SYAP1 antibody (AA 151-230) (Biotin)

Catalog No. ABIN725287

Product Details anti-SYAP1 Antibody (Biotin)

Target: SYAP1 (Synapse Associated Protein 1 (SYAP1))

Binding Specificity: AA 151-230

Reactivity: Human, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SYAP1 antibody is conjugated to Biotin

Application: Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Cross-Reactivity: Human, Rat

Predicted Reactivity: Mouse,Dog,Cow,Pig,Horse,Chicken

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human SYAP1

Isotype: IgG

Application Details

Application Notes: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % 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: -20 °C

Storage Comment: Store at -20°C for 12 months.

Expiry Date: 12 months

Target Details for SYAP1

Target: SYAP1 (Synapse Associated Protein 1 (SYAP1))

Alternative Name: SYAP1 (SYAP1 Products)

Synonyms: 2010110O17Rik antibody, AW011796 antibody, synapse associated protein 1 antibody, SYAP1 antibody, Syap1 antibody

Background:

Synonyms: PRO3113, Synapse-associated protein 1, SYAP1

Background: SYAP1 (synapse-associated protein 1) is a 352 amino acid protein that is ubiquitously expressed in adult tissues. SYAP1 contains one BSD domain which is a novel domain that is present in basal transcription factors, synapse-associated proteins and several hypothetical proteins. The BSD domain is characterized by three predicted alpha helices and by conserved tryptophan and phenylalanine residues, located at the C-terminus of the domain. The gene that encodes SYAP1 in humans is located on chromosome X. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.

Gene ID: 94056

UniProt: Q96A49