STAMBPL1 antibody (AA 187-436) (FITC)
Quick Overview for STAMBPL1 antibody (AA 187-436) (FITC) (ABIN8042501)
Target
See all STAMBPL1 AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- AA 187-436
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Purpose
- Anti-AMSH-LP/STAMBPL1 Antibody FITC Conjugated
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Cross-Reactivity (Details)
- No cross-reactivity with other proteins.
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Purification
- Immunogen affinity purified.
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Immunogen
- E.coli-derived human AMSH-LP/STAMBPL1 recombinant protein (Position: Q187-R436).
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Isotype
- IgG
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Application Notes
- Flow Cytometry, Optimal dilutions should be determined by end users.
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Restrictions
- For Research Use only
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Format
- Liquid
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Buffer
- Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 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
- At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.
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Expiry Date
- 12 months
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- STAMBPL1 (STAM Binding Protein-Like 1 (STAMBPL1))
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Alternative Name
- STAMBPL1
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Background
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Background: STAMBPL1 (STAM-binding protein-like 1), also known as AMSH-FP, AMSH-LP (associated molecule with the SH3 domain of STAM like protein) or ALMa, is a 436 amino acid protein that belongs to the peptidase M67C family, contains one MPN domain and a JAMM motif that is essential for protease activity. Existing as two alternatively spliced isoforms, STAMBPL1 is a ubiquitously expressed protein that binds two zinc ions per subunit and acts as a zinc metalloprotease that specifically cleaves Lys-63-linked polyubiquitin chains. The gene that encodes STAMBPL1 maps to human chromosome 10q23.31. Chromosome 10 contains over 800 genes and 135 million nucleotides, making up nearly 4.5 % of the human genome. PTEN is an important tumor suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. The chromosome 10 encoded gene ERCC6 is important for DNA repair and is linked to Cockayne syndrome which is characterized by extreme photosensitivity and premature aging. Tetrahydrobiopterin deficiency and a number of syndromes involving defective skull and facial bone fusion are also linked to chromosome 10.
Gene Full Name: STAM binding protein like 1
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Gene ID
- 57559
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UniProt
- Q96FJ0
Target
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