SIM1 antibody (Middle Region)
-
- Target See all SIM1 Antibodies
- SIM1 (Single-Minded Homolog 1 (SIM1))
-
Binding Specificity
- Middle Region
-
Reactivity
- Human, Cow, Dog, Horse, Mouse, Rabbit, Rat, Guinea Pig, Pig
-
Host
- Rabbit
-
Clonality
- Polyclonal
-
Conjugate
- This SIM1 antibody is un-conjugated
-
Application
- Immunohistochemistry (IHC)
- Sequence
- SSSKSKSRTS PYPQYSGFHT ERSESDHDSQ WGGSPLTDTA SPQLLDPADR
- Predicted Reactivity
- Cow: 93%, Dog: 100%, Guinea Pig: 93%, Horse: 100%, Human: 100%, Mouse: 100%, Pig: 100%, Rabbit: 100%, Rat: 100%
- Characteristics
- This is a rabbit polyclonal antibody against SIM1. It was validated on Western Blot.
- Purification
- Affinity Purified
- Immunogen
- The immunogen is a synthetic peptide directed towards the middle region of Human SIM1
- Top Product
- Discover our top product SIM1 Primary Antibody
-
-
- Application Notes
- Optimal working dilutions should be determined experimentally by the investigator.
- Comment
-
Antigen size: 766 AA
- Restrictions
- For Research Use only
-
- Format
- Liquid
- Concentration
- Lot specific
- Buffer
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
- Preservative
- Sodium azide
- Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Handling Advice
- Avoid repeated freeze-thaw cycles.
- Storage
- -20 °C
- Storage Comment
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
-
- Target
- SIM1 (Single-Minded Homolog 1 (SIM1))
- Alternative Name
- SIM1 (SIM1 Products)
- Background
-
SIM1 and SIM2 genes are Drosophila single-minded (sim) gene homologs. SIM1 transcript was detected only in fetal kidney out of various adult and fetal tissues tested. Since the sim gene plays an important role in Drosophila development and has peak levels of expression during the period of neurogenesis,it was proposed that the human SIM gene is a candidate for involvement in certain dysmorphic features (particularly the facial and skull characteristics), abnormalities of brain development, and/or mental retardation of Down syndrome.
Alias Symbols: bHLHe14
Protein Interaction Partner: ARNT, HSP90AA1,
Protein Size: 766 - Molecular Weight
- 85 kDa
- Gene ID
- 6492
- NCBI Accession
- NM_005068, NP_005059
- UniProt
- P81133
-