NSG2 antibody (AA 31-140) (AbBy Fluor® 680)
-
- Target See all NSG2 (HMP19) Antibodies
- NSG2 (HMP19) (Neuron-Specific Protein Family Member 2 (HMP19))
-
Binding Specificity
- AA 31-140
-
Reactivity
- Human
-
Host
- Rabbit
-
Clonality
- Polyclonal
-
Conjugate
- This NSG2 antibody is conjugated to AbBy Fluor® 680
-
Application
- Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Predicted Reactivity
- Human,Mouse,Rat,Cow,Pig,Chicken,Rabbit
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human NSG2/HMP19
- Isotype
- IgG
- Top Product
- Discover our top product HMP19 Primary Antibody
-
-
- Application Notes
-
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - Restrictions
- For Research Use only
-
- 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Expiry Date
- 12 months
-
- Target
- NSG2 (HMP19) (Neuron-Specific Protein Family Member 2 (HMP19))
- Alternative Name
- NSG2 (HMP19 Products)
- Synonyms
- NSG2 antibody, 8.5 antibody, AA989750 antibody, R75287 antibody, neuronal vesicle trafficking associated 2 antibody, neuron specific gene family member 2 antibody, NSG2 antibody, Nsg2 antibody
- Background
-
Synonyms: HMP19, Neuron-specic protein family member 2, Nsg2, NSG2_HUMAN, Protein p19.
Background: With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6 % of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.
-