COL4a3 antibody (Middle Region)
Quick Overview for COL4a3 antibody (Middle Region) (ABIN2788301)
Target
See all COL4a3 (COL4A3) AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- Middle Region
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Purpose
- COL4A3 Antibody - middle region
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Sequence
- DPGQPGPPGE QGPPGRCIEG PRGAQGLPGL NGLKGQQGRR GKTGPKGDPG
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Predicted Reactivity
- Cow: 93%, Dog: 91%, Guinea Pig: 86%, Horse: 93%, Human: 100%, Mouse: 91%, Pig: 93%, Rabbit: 85%, Rat: 91%
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Characteristics
- This is a rabbit polyclonal antibody against COL4A3. It was validated on Western Blot.
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Purification
- Affinity Purified
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Immunogen
- The immunogen is a synthetic peptide directed towards the middle region of human COL4A3
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Application Notes
- Optimal working dilution should be determined by the investigator.
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Comment
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We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP60006-100UG
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 0.5 mg/mL
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Buffer
- Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
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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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Handling Advice
- prevent freeze-thaw cycles
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Storage
- 4 °C,-20 °C
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Storage Comment
- For short term use, store at 2-8C up to 1 week. For long term storage, store at -20 °C in small aliquots to prevent freeze-thaw cycles.
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- COL4a3 (COL4A3) (Collagen, Type IV, alpha 3 (COL4A3))
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Alternative Name
- COL4A3
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Background
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Background Information: Type IV collagen, the major structural component of basement membranes, is a multimeric protein composed of 3 alpha subunits. These subunits are encoded by 6 different genes, alpha 1 through alpha 6, each of which can form a triple helix structure with 2 other subunits to form type IV collagen. This gene encodes alpha 3. In the Goodpasture syndrome, autoantibodies bind to the collagen molecules in the basement membranes of alveoli and glomeruli. The epitopes that elicit these autoantibodies are localized largely to the non-collagenous C-terminal domain of the protein. A specific kinase phosphorylates amino acids in this same C-terminal region and the expression of this kinase is upregulated during pathogenesis. There are multiple alternate transcripts that appear to be unique to this human alpha 3 gene and alternate splicing is restricted to the six exons that encode this C-terminal domain. This gene is also linked to an autosomal recessive form of Alport syndrome. The mutations contributing to this syndrome are also located within the exons that encode this C-terminal region. Like the other members of the type IV collagen gene family, this gene is organized in a head-to-head conformation with another type IV collagen gene so that each gene pair shares a common promoter. Some exons of this gene are interspersed with exons of an uncharacterized gene which is on the opposite strand.
Gene Name: Collagen, type IV, alpha 3 (Goodpasture antigen)
Alternative Symbols: ATS2, ATS3
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Molecular Weight
- 156kDa
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Gene ID
- 1285
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NCBI Accession
- NP_112730
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UniProt
- E7ENN2
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Pathways
- Sensory Perception of Sound, Positive Regulation of Endopeptidase Activity
Target
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