ESYT1 antibody (AA 651-750)
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- Target See all ESYT1 Antibodies
- ESYT1 (Extended Synaptotagmin-Like Protein 1 (ESYT1))
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Binding Specificity
- AA 651-750
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Reactivity
- Human, Mouse
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This ESYT1 antibody is un-conjugated
- Application
- Western Blotting (WB), 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))
- Cross-Reactivity
- Human, Mouse
- Predicted Reactivity
- Rat,Dog,Cow,Pig,Horse,Rabbit,Monkey
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human ESYT1/FAM62A
- Isotype
- IgG
- Top Product
- Discover our top product ESYT1 Primary Antibody
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- Application Notes
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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
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- 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
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- Target
- ESYT1 (Extended Synaptotagmin-Like Protein 1 (ESYT1))
- Alternative Name
- ESYT1/FAM62A (ESYT1 Products)
- Synonyms
- FAM62A antibody, fam62a antibody, si:ch211-239j9.4 antibody, DKFZp459I1628 antibody, MBC2 antibody, Fam62a antibody, Mbc2 antibody, vp115 antibody, extended synaptotagmin 1 antibody, extended synaptotagmin-like protein 1b antibody, extended synaptotagmin-like protein 1 antibody, ESYT1 antibody, esyt1b antibody, Esyt1 antibody
- Background
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Synonyms: Extended synaptotagmin 1, KIAA0747, E Syt1, E-Syt1, Esyt1, ESYT1_HUMAN, Extended synaptotagmin like protein 1, Extended synaptotagmin-1, Family with sequence similarity 62 C2 domain containing member A, Family with sequence similarity 62 member A, MBC2, Membrane bound C2 domain containing protein, Membrane-bound C2 domain-containing protein, Protein FAM62A.
Background: Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5 % of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The FAM62A gene product has been provisionally designated FAM62A pending further characterization.
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