NSMCE2 antibody (AA 30-110)
Quick Overview for NSMCE2 antibody (AA 30-110) (ABIN7219926)
Target
See all NSMCE2 AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- AA 30-110
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Purpose
- NSE2 Polyclonal Antibody
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Specificity
- NSE2 Polyclonal Antibody detects endogenous levels of NSE2 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 N-terminal region of human NSE2 at AA range: 30-110
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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 (1:10000). 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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- NSMCE2 (E3 SUMO-Protein Ligase NSE2 (NSMCE2))
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Alternative Name
- NSE2
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Background
- Rabbit Anti-NSE2 Polyclonal Antibody,FAM84B, BCMP101, NSE2, Protein FAM84B, Breast cancer membrane protein 101, Protein NSE2,FAM84B (family with sequence similarity 84, member B), also known as NSE2 or BCMP101, is a 310 amino acid protein that is expressed in esophageal squamous cell carcinomas, suggesting a role in tumor development and metastasis. The gene encoding FAM84B maps to human chromosome 8, which consists of nearly 146 million base pairs, houses more than 800 genes and is associated with a variety of diseases and malignancies. Schizophrenia, bipolar disorder, trisomy 8, Pfeiffer syndrome, congenital hypothyroidism, Waardenburg syndrome and some leukemias and lymphomas are thought to occur as a result of defects in specific genes that map to chromosome 8.,Protein FAM84B
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Molecular Weight
- observerd band 38kDa
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Gene ID
- 157638
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UniProt
- Q96KN1
Target
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