Anti-TRIM32/BBS11 (Polyclonal), ALEXA Fluor 594

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Catalog number: GENTAUR-58be5a0548872
Price: 489 €
Supplier: Bioss Polyclonal Antibodies
Product name: Anti-TRIM32/BBS11 (Polyclonal), ALEXA Fluor 594
Quantity: 100 microliters
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Type: Conjugated Primary Antibody
Conjugated with: 594, ALEXA FLUOR®
Host organism: Rabbit (Oryctolagus cuniculus)
Target Protein/Peptide: TRIM32/BBS11
Specificity: This antibody reacts specifically with TRIM32/BBS11
Modification: No modification has been applied to this antibody
Modification site: None
Clonality: Polyclonal Antibody
Clone: Polyclonal Antibodies
Concentration: 1ug per 1ul
Antigen Source: KLH conjugated synthetic peptide derived from mouse TRIM32
Gene ID: 22954
Applications: IF(IHC-P)
Applications with corresponding dilutions: IF(IHC-P)(1:50-200)
Cross reactive species: Mouse (Mus musculus), Rat (Rattus norvegicus), Human (Homo sapiens)
Cross Reactive Species details: However, note that due to limited knowledge it is impossible to predict with 100% guarantee that the antibody does not corss react with any other species, No significant cross reactivity has been observed for this antibody for the tested species
Background information: Additionally, Mutations in the TRIM32 gene cause two forms of autosomal recessive muscular dystrophy designated limb girdle muscular dystrophy type 2H (LGMD2H) and sarcotubular myopathy (STM), TRIM32, TRIM32 has six C-terminal NHL domains, TRIM32 mutations can also result in Bardet-Biedl syndrome (BBS), The TRIM32 gene encodes an E3 ubiquitin ligase, UbcH5c and UbcH6, a RING-finger and a coiled-coil motif, a protein that attaches ubiquitin to a lysine residue on a target protein and acts in conjunction with ubiquitin-conjugating enzymes UbcH5a, an autosomal recessive disorder characterized by pigmentary retinopathy, contains a domain structure composed of a B-box, hypogenitalism, it is expressed mainly in the skeletal muscle, learning disabilities and obesity, like all TRIM proteins, polydactyly, renal abnormalities, Tripartite motif-containing protein 32 (TRIM32) belongs to the tripartite motif (TRIM) protein family
Purification method: Purified by Protein A
Storage: 50% glycerol and 0, Store at 4°, 09% sodium azide, C for 12 months, Water buffered solution containing 100ug/ml BSA
Excitation emission: 590nm/617nm
Synonyms: HT2A TATIP BBS11
Also known as: TRIM32/BBS11 Polyclonal Antibody
Other name: Anti-TRIM32/BBS11 Polyclonal
Advisory: For antibodies that are in liquid form or reconstituted lyophilized antibodies small amounts could become entrapped on the seal or the walls of the tube, Prior to use briefly centrifuge the vial to gather all the solution on the bottom, specificity and sensitivity, thus reducing its reactivity, Avoid freeze/thaw cycles as they may denaturate the polypeptide chains of the antibody
Properties: For facs or microscopy Alexa 1 conjugate
Conjugation: Alexa Fluor
Group: Polyclonals and antibodies
About: The advantage is that there are more epitopes available in a polyclonal antiserum to detect the proteins than in monoclonal sera, immunohistochemistry on frozen slices or parrafin fixed tissues, Polyclonals can be used for Western blot
Gene target: TRIM32/BBS11
Short name: Anti-TRIM32/BBS11 (Polyclonal) Fluor 594
Technique: Pabs are a collection of immunoglobulin , Polyclonal antibodies , each identifying a different , whereas , (pAbs) are mostly rabbit or goat , B cells, Polyclonal, antibodies , antigen, come from a single N cell lineage, epitope, molecules that react against a specific , monoclonal antibodies , that are secreted by different 
Label: ALEXA
Alternative name: ALEXA Fluor 594, antibody to-TRIM32/BBS11 (polyclonal)
Alternative technique: polyclonals
Identity: 16380
Gene: TRIM32 | More about : TRIM32
Long gene name: tripartite motif containing 32
Synonyms gene: LGMD2H
Synonyms gene name: limb girdle muscular dystrophy 2H (autosomal recessive) tripartite motif-containing 32
Locus: 9q33, 1
Discovery year: 2001-08-10
GenBank acession: U18543
Entrez gene record: 22954
Pubmed identfication: 11331580 7778269 16606853
RefSeq identity: NM_012210
Classification: Tripartite motif containing Ring finger proteins Bardet-Biedl syndrome associated
Havana BLAST/BLAT: OTTHUMG00000021026
Locus Specific Databases: Leiden Muscular Dystrophy Pages Leiden Muscular Dystrophy pages LRG_211

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