SYAP1 antibody (AA 151-230)
Quick Overview for SYAP1 antibody (AA 151-230) (ABIN725285)
Target
Reactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- AA 151-230
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Cross-Reactivity
- Human, Rat
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Predicted Reactivity
- Mouse,Dog,Cow,Pig,Horse,Chicken
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Purification
- Purified by Protein A.
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Immunogen
- KLH conjugated synthetic peptide derived from human SYAP1
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Isotype
- IgG
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Application Notes
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WB 1:300-5000
ELISA 1:500-1000
FCM 1:20-100
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 -
Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 μg/μL
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Buffer
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
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Preservative
- ProClin
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Precaution of Use
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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Storage
- 4 °C,-20 °C
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Storage Comment
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
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Expiry Date
- 12 months
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: "Isolation and characterization of chicken dermis-derived mesenchymal stem/progenitor cells." in: BioMed research international, Vol. 2013, pp. 626258, (2013) (PubMed).
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: "Isolation and characterization of chicken dermis-derived mesenchymal stem/progenitor cells." in: BioMed research international, Vol. 2013, pp. 626258, (2013) (PubMed).
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- SYAP1 (Synapse Associated Protein 1 (SYAP1))
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Alternative Name
- SYAP1
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Background
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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.
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Gene ID
- 94056
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UniProt
- Q96A49
Target
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