IFT122 antibody (Middle Region)
Quick Overview for IFT122 antibody (Middle Region) (ABIN8103429)
Target
See all IFT122 AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- Middle Region
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Purpose
- IFT122 Antibody - middle region
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Sequence
- QDLRYLELIS SIEERKKRGE TNNDLFLADV FSYQGKFHEA AKLYKRSGHE
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Predicted Reactivity
- Cow: 100%, Dog: 100%, Guinea Pig: 100%, Horse: 100%, Human: 100%, Mouse: 100%, Rabbit: 100%, Rat: 100%, Zebrafish: 93%
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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 IFT122
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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 AAP53816-100UG
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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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- IFT122 (Intraflagellar Transport 122 (IFT122))
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Alternative Name
- IFT122
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Background
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Background Information: This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This cytoplasmic protein contains seven WD repeats and an AF-2 domain which function by recruiting coregulatory molecules and in transcriptional activation. Mutations in this gene cause cranioectodermal dysplasia-1. A related pseudogene is located on chromosome 3. Alternative splicing results in multiple transcript variants encoding different isoforms.
Gene Name: intraflagellar transport 122
Alternative Symbols: CED, SPG, CED1, FAP80, WDR10, WDR10p, WDR140
Protein Name: Intraflagellar transport protein 122 homolog
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Molecular Weight
- 130 kDa
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Gene ID
- 55764
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NCBI Accession
- NP_443715
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UniProt
- Q9HBG6
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Pathways
- Tube Formation, Embryonic Body Morphogenesis
Target
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