Homeobox D13 antibody (N-Term)
Quick Overview for Homeobox D13 antibody (N-Term) (ABIN5516975)
Target
See all Homeobox D13 (HOXD13) AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- N-Term
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Purpose
- HOXD13 Antibody - N-terminal region
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Sequence
- ASGFAYPGTS ERTGSSSSSS SSAVVAARPE APPAKECPAP TPAAAAAAPP
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Characteristics
- This is a rabbit polyclonal antibody against HXD13. It was validated on Western Blot.
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Purification
- Affinity purified
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Immunogen
- The immunogen for Anti-HOXD13 antibody is: synthetic peptide directed towards the N-terminal region of Human HXD13
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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 AAP76277-100UG
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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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- Homeobox D13 (HOXD13)
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Alternative Name
- HOXD13
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Background
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Background Information: This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, located on different chromosomes, consisting of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXD genes located in a cluster on chromosome 2. Deletions that remove the entire HOXD gene cluster or the 5' end of this cluster have been associated with severe limb and genital abnormalities. Mutations in this particular gene cause synpolydactyly.
Gene Name: homeobox D13
Alternative Symbols: BDE, SPD, BDSD, SPD1, HOX4I
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Molecular Weight
- 37 kDa
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Gene ID
- 3239
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NCBI Accession
- NP_000514
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UniProt
- P35453
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Pathways
- Synaptic Membrane
Target
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