货号:AB5228-200UL
品牌:Merck Millipore
规格:1EA
目录价:¥8390.71
市场价格:¥7132.10
会员价格:¥6712.57
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Description:
Anti-Potassium Channel MaxiK Antibody, calcium activated, aa1097-1196 | AB5228-200UL
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Promotional Text:
Special Shipping Offer on Antibodies100% Performance Guaranteed
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Trade Name:
Chemicon (Millipore)
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Specificity:
Corresponds to the C-terminus of the longer form of BKCa channel α subunit and overlaps by ~40 residues with a shorter form and not with other known proteins tested so far.
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Epitope:
C-terminal sequence SHSSHSSQ
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Immunogen:
A purified fusion protein (GST) and a C-terminal part (residues 1097-1196) of mouse KCa1.1 channel (Accession Q08460-2).
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Species Reactivity:
Rat
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Application Notes:
Western blot: 1:200 using ECL on rat brain membranes.Note: The addition of 0.1% Tween to the standard milk block is recommended.Immunohistochemistry on rat brain sections.Dilutions should be made using a carrier protein such as BSA (1-3%)Optimal working dilutions must be determined by the end user.
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Control:
CONTROL ANTIGEN: Included free of charge with the antibody is 50 μg of control antigen (lyophilized powder in phosphate buffered saline, pH 7.4, containing 5% sucrose and 0.025% sodium azide). The stock solution of the antigen can be made up using 100 μL of sterile deionized water. For positive control, in Western blotting, use 20 ng protein per lane. For negative control, preincubate 3-5 μg of purified peptide with 1 μg of antibody for one hour at room temperature. Optimal concentrations must be determined by the end user.
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Presentation:
Affinity purified immunoglobulin. Lyophilized from phosphate buffered saline, pH 7.4, containing 1% BSA, 5% sucrose as a stabilizer and 0.025% sodium azide as a preservative. Reconstitute with 200 μL of sterile deionized water. Centrifuge antibody preparation before use (10,000 xg five minutes).
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Storage Conditions:
Maintain lyophilized material at -20°C for up to 12 months. After reconstitution maintain at -20°C in undiluted aliquots for up to 6 months. Avoid repeated freeze/thaw cycles.
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UniProt Number:
Q12791
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Entrez Gene Number:
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NM_001014797.1
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NM_002247.2
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Gene Symbol:
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KCNMA1
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OTTHUMP00000064161
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OTTHUMP00000060198
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KCNMA
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K
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OTTHUMP00000064158
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MaxiK
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VCAlpha)
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SLO-ALPHA
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MGC71881
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OTTHUMP00000064157
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SAKCA
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OTTHUMP00000064156
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OTTHUMP00000064164
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Slo1
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BKTM
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OTTHUMP00000064165
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hSlo
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mSLO1
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OTTHUMP00000064154
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Slo-alpha
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SLO
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OTTHUMP00000064162
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KCa1.1
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OTTHUMP00000064155
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OTTHUMP00000064160
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DKFZp686K1437
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OTTHUMP00000064159
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Alternate Names:
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BKCa; Slo; KCNMA1
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KCa1.1
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Usage Statement:
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
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Key Applications:
Western Blotting
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Entrez Gene Summary:
MaxiK channels are large conductance, voltage and calcium-sensitive potassium channels which are fundamental to the control of smooth muscle tone and neuronal excitability. MaxiK channels can be formed by 2 subunits: the pore-forming alpha subunit, which is the product of this gene, and the modulatory beta subunit. Intracellular calcium regulates the physical association between the alpha and beta subunits. Alternatively spliced transcript variants encoding different isoforms have been identified.
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UniProt Summary:
FUNCTION: SwissProt: Q12791 # Potassium channel activated by both membrane depolarization or increase in cytosolic Ca(2+) that mediates export of K(+). It is also activated by the concentration of cytosolic Mg(2+). Its activation dampens the excitatory events that elevate the cytosolic Ca(2+) concentration and/or depolarize the cell membrane. It therefore contributes to repolarization of the membrane potential. Plays a key role in controlling excitability in a number of systems, such as regulation of the contraction of smooth muscle, the tuning of hair cells in the cochlea, regulation of transmitter release, and innate immunity. In smooth muscles, its activation by high level of Ca(2+), caused by ryanodine receptors in the sarcoplasmic reticulum, regulates the membrane potential. In cochlea cells, its number and kinetic properties partly determine the characteristic frequency of each hair cell and thereby helps to establish a tonotopic map. Kinetics of KCNMA1 channels are determined by alternative splicing, phosphorylation status and its combination with modulating beta subunits. Highly sensitive to both iberiotoxin (IbTx) and charybdotoxin (CTX).SIZE: 1236 amino acids; 137560 Da SUBUNIT: Homotetramer; which constitutes the calcium-activated potassium channel. Interacts with beta subunits KCNMB1, KCNMB2, KCNMB3 and KCNMB4. Beta subunits are accessory, and modulate its activity.SUBCELLULAR LOCATION: Membrane; Multi-pass membrane protein.TISSUE SPECIFICITY: Widely expressed. Except in myocytes, it is almost ubiquitously expressed.DOMAIN: SwissProt: Q12791 The S0 segment is essential for the modulation by the accessory beta subunits KCNMB1, KCNMB2, KCNMB3 and KCNMB4. & The S4 segment, which is characterized by a series of positively charged amino acids at every third position, is part of the voltage-sensor. & The pore-forming domain (also referred as P region) is imbedded into the membrane, and forms the selectivity filter of the pore. It contains the signature sequence of potassium channels that displays selectivity to potassium. & The RCK N-terminal domain mediates the homotetramerization, thereby promoting the assembly of monomers into functional potassium channel. It includes binding sites for Ca(2+) and Mg(2+) (By similarity). & The calcium bowl constitutes one of the Ca(2+) sensors and probably acts as a Ca(2+)-binding site. There are however other Ca(2+) sensors regions required for activation of the channel.PTM: Phosphorylated (Probable). Phosphorylation by kinases such as PKA and/or PKG. In smooth muscles, phosphorylation affects its activity.DISEASE: SwissProt: Q12791 # Defects in KCNMA1 are the cause of generalized epilepsy and paroxysmal dyskinesia (GEPD) [MIM:609446]. Epilepsy is one of the most common and debilitating neurological disorders, affecting more than 40 million people worldwide. Paroxysmal dyskinesias are another heterogeneous group of neurological disorders characterized by sudden, unpredictable, disabling attacks of involuntary movement often requiring life-long treatment. The coexistence of epilepsy and paroxysmal dyskinesia in the same individual or family is an increasingly recognized phenomenon. The basic pathophysiology underlying the coexistence of these two disorders is caused by mutations in the KCNMA1 gene.SIMILARITY: Belongs to the potassium channel family. Calcium- activated subfamily. & Contains 1 RCK N-terminal domain.MISCELLANEOUS: The protein was initially thought to contain two functionally distinct parts: The core channel (from the N-terminus to the S9 segment) that mediates the channel activity, and the cytoplasmic tail (from the S9 segment to the C-terminus) that mediates the calcium sensing. The situation is however more complex, since the core channel also contains binding sites for Ca(2+) and Mg(2+).
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Brand Family:
Chemicon
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Product Name:
Anti-Potassium Channel MaxiK Antibody, calcium activated, aa1097-1196 | AB5228-200UL
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Concentration:
60 μg/200 μL (after reconstitution)
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Antibody Type:
Polyclonal Antibody
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Qty/Pk:
200 µL
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Format:
Affinity Purified
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Host:
Rabbit
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