GOLPH3 antibody (AA 51-150) (FITC)
Quick Overview for GOLPH3 antibody (AA 51-150) (FITC) (ABIN1709761)
Target
See all GOLPH3 AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- AA 51-150
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Cross-Reactivity
- Human
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Predicted Reactivity
- Mouse,Rat,Dog,Cow,Horse,Chicken
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Purification
- Purified by Protein A.
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Immunogen
- KLH conjugated synthetic peptide derived from human GOLPH3
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Isotype
- IgG
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Application Notes
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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
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % 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
- -20 °C
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Storage Comment
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
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Expiry Date
- 12 months
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- GOLPH3 (Golgi phosphoprotein 3 (Coat-Protein) (GOLPH3))
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Alternative Name
- GOLPH3
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Background
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Synonyms: Coat protein, Coat protein GPP34, FLJ90675, Golgi associated protein, Golgi peripheral membrane protein 1, 34 kDa, Golgi phosphoprotein 3 coat protein, Golgi phosphoprotein 3, Golgi protein, GOLP3_HUMAN, Golph3, GOPP1, GPP34, MIDAS, Mitochondrial DNA absence factor.
Background: The Golgi complex plays a key role in the sorting and modification of proteins exported from the endoplasmic reticulum. GOLPH3L (golgi phosphoprotein 3-like), also known as GPP34R, is a 285 amino acid cytoplasmic protein that localizes to the Golgi apparatus. Belonging to the GOLPH3/VPS74 family, GOLPH3L may have a regulatory role in Golgi trafficking. GOLPH3L is encoded by a gene located on human chromosome 1, which spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8 % of the human genome. Chromosome 1 houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson?s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma.
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Gene ID
- 64083
Target
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