NBPF1,9,10,12,14,15,16,20 (AA 700-780) antibody
Quick Overview for NBPF1,9,10,12,14,15,16,20 (AA 700-780) antibody (ABIN7215966)
Target
Reactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- AA 700-780
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Purpose
- NBPF1/9/10/12/14/15/16/20 Polyclonal Antibody
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Specificity
- NBPF1/9/10/12/14/15/16/20 Polyclonal Antibody detects endogenous levels of NBPF1/9/10/12/14/15/16/20 protein.
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Purification
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen
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Immunogen
- Synthesized peptide derived from the C-terminal region of human NBPF1/9/10/12/14/15/16/20 at AA range: 700-780
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Isotype
- IgG
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Application Notes
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), IHC-P (1:100-1:300), ELISA (1:40000). Not yet tested in other applications.
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Comment
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Primary Antibody
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 mg/mL
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Buffer
- PBS containing 50 % Glycerol, 0.5 % BSA and 0.02 % Sodium Azide.
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Preservative
- Sodium azide
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Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Storage
- -20 °C
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Storage Comment
- Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
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- NBPF1,9,10,12,14,15,16,20
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Alternative Name
- NBPF1/9/10/12/14/15/16/20
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Background
- Rabbit Anti-NBPF1/9/10/12/14/15/16/20 Polyclonal Antibody,NBPF12, COAS1, KIAA1245, Neuroblastoma breakpoint family member 12, Chromosome 1 amplified sequence 1, NBPF10, Neuroblastoma breakpoint family member 10, NBPF16, Neuroblastoma breakpoint family member 16, NBPF1, KIAA1693, Neuroblastoma brea,NBPF1 is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1. This gene family has experienced its greatest expansion within the human lineage and has expanded, to a lesser extent, among primates in general. Members of this gene family are characterized by tandemly repeated copies of DUF1220 protein domains. Gene copy number variations in the human chromosomal region 1q21. , where most DUF1220 domains are located, have been implicated in a number of developmental and neurogenetic diseases such as microcephaly, macrocephaly, autism, schizophrenia, mental retardation, congenital heart disease, neuroblastoma, and congenital kidney and urinary tract anomalies. Altered expression of some gene family members is associated with several types of cancer. This gene family contains numerous pseudogenes.,Neuroblastoma breakpoint family member 12
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Molecular Weight
- observerd band 36kDa
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Gene ID
- 55672, 400818, 284565
Target
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