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MID1 Antibody

Hersteller ProSci
Kategorie
Typ Antibody Polyclonal
Specific against Human, Mouse, Rat, Canine, Carp
Format Liquid
Applikationen WB, ELISA
Menge 100 ul
Host Rabbit
ArtNr PRS-28-162-100ul
eClass 6.1 32160702
eClass 9.0 32160702
Lieferbar
Shipping
blue ice or RT
By Research Area
Transcription
Immunogen
Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human MID1.
Applications
MID1 antibody can be used for detection of MID1 by ELISA at 1:312500. MID1 antibody can be used for detection of MID1 by western blot at 2.5 μ g/mL, and HRP conjugated secondary antibody should be diluted 1:50, 000 - 100, 000.
Positive Control 1
Cat. No. 1205 - Jurkat Cell Lysate
Predicted Molecular Weight
75 kDa, 75 kDa, 62 kDa
Purification
Antibody is purified by protein A chromatography method.
Clonality
Polyclonal
Conjugate
Unconjugated
Buffer
Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
Concentration
batch dependent
Storage Conditions
For short periods of storage (days) store at 4˚ C. For longer periods of storage, store MID1 antibody at -20˚ C. As with any antibody avoid repeat freeze-thaw cycles.
Disclaimer
This product is for research use only.
Modifications
None
Ncbi Official Symbol
MID1
Accession #
NP_000372
Protein Gi #
4557753
Ncbi Gene Id #
4281
User Note
Optimal dilutions for each application to be determined by the researcher.
Ncbi Official Symbol
MID1
Ncbi Official Full Name
midline 1 (Opitz/BBB syndrome)
Ncbi Organism
Homo sapiens
Swissprot #
O15344
Background
MID1 is a member of the tripartite motif (TRIM) family, also known as the 'RING-B box-coiled coil' (RBCC) subgroup of RING finger proteins. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein forms homodimers which associate with microtubules in the cytoplasm. The protein is likely involved in the formation of multiprotein structures acting as anchor points to microtubules. Mutations in this gene have been associated with the X-linked form of Opitz syndrome, which is characterized by midline abnormalities such as cleft lip, laryngeal cleft, heart defects, hypospadias, and agenesis of the corpus callosum. This gene was also the first example of a gene subject to X inactivation in human while escaping it in mouse. Several different transcript variants are generated by alternate splicing; however, the full length nature of two variants has not been determined.
Background References 1
Winter, J., et al., (2004) Hum. Genet. 114 (6), 541-552.
1st Image Caption
Antibody used in WB on Human Jurkat 2.5 ug/ml.

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Alle Produkte sind nur für Forschungszwecke bestimmt. Nicht für den menschlichen, tierärztlichen oder therapeutischen Gebrauch.

Menge: 100 ul
Lieferbar: In stock
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Lieferung vsl. bis 04.07.2024 

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