| Long name: |
TRIM32/BBS11 Primary Polyclonal Antibody |
| Also known as: |
TRIM32/BBS11 PAb |
| Category: |
Primary Antibodies |
| Conjugation: |
Unconjugated |
| Target Antigen: |
TRIM32/BBS11 |
| Specificity: |
This is a highly specific antibody against TRIM32/BBS11 |
| Modification(s): |
None |
| Modification site(s): |
Unmodified antibody |
| Clonality: |
Polyclonal antibody |
| Clone number: |
Polyclonal antibody |
| Concentration: |
1ug per 1ul |
| Source: |
KLH conjugated synthetic peptide derived from mouse TRIM32 |
| Gene ID number: |
22954 |
| Tested Applications: |
IF(IHC-P), IHC-P, WB |
| Recommended dilutions: |
IF(IHC-P)(1:50-200), IHC-P(1:100-500), WB(1:100-1000) |
| Cross reactivity: |
Mouse, Rat, Human |
| Cross reactive species details: |
not every possible cross-reactivity is known, Due to limited amount of testing and knowledge |
| Background of the target antigen: |
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: |
This antibody was purified via Protein A |
| Storage conditions: |
50% glycerol and 0, Store at -20°, 09% sodium azide, C for up to 1 year, Keep the antibody in aqueous buffered solution containing 1% BSA |
| Synonym names: |
BBS11, HT2A, LGMD2H, Limb girdle muscular dystrophy 2H, Limb girdle muscular dystrophy 2H autosomal recessive, Muscular dystrophy Hutterite type, TAT interactive protein 72KD, TATIP, TRI32_MOUSE, Tripartite Mot Containing Protein 32, Zinc Finger Protein HT2A, 72 kda Tat interacting Protein |
| Properties: |
C, C for long term storage and for short term at + 5°, If you buy Antibodies supplied by Bioss Primary Unconjugated Antibodies they should be stored frozen at - 24° |
| Gene target: |
TRIM32/BBS11 |
| Short name: |
TRIM32/BBS11 Antibody |
| Technique: |
antibodies against human proteins, antibodies for, Antibody |
| Alternative name: |
TRIM32/BBS11 (Antibody to) |
| Alternative technique: |
antibodies |
| 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 |
| Synonyms: |
HT2A TATIP BBS11 |
| 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 |