| Long name: |
Cy3 Conjugated, Dysferlin Polyclonal Antibody |
| Category: |
Conjugated Primary Antibodies |
| Conjugation: |
cy3 conjugation kit |
| Host Organism: |
Rabbit (Oryctolagus cuniculus) |
| Target Antigen: |
Dysferlin |
| Specificity: |
This is a highly specific antibody against Dysferlin |
| Modification: |
Unmodified |
| Modification site: |
None |
| Clonality: |
Polyclonal |
| Clone: |
Polyclonal antibody |
| Concentration: |
1ug per 1ul |
| Source: |
KLH conjugated synthetic peptide derived from human Dysferlin |
| Gene ID number: |
8291 |
| Tested applications: |
IF(IHC-P) |
| Recommended dilutions: |
IF(IHC-P)(1:50-200) |
| Crossreactivity: |
Mouse, Rat, Human |
| Crossreactive species details: |
not every possible cross-reactivity is known, Due to limited amount of testing and knowledge |
| Antigen background: |
Alternative splicing results in multiple transcript variants, Aug 2008], In addition, It is involved in muscle contraction and contains C2 domains that play a role in calcium-mediated membrane fusion events, Specific mutations in this gene have been shown to cause autosomal recessive limb girdle muscular dystrophy type 2B (LGMD2B) as well as Miyoshi myopathy, [provided by RefSeq, a skeletal muscle membrane protein which is important in the formation of caveolae, suggesting that it may be involved in membrane regeneration and repair, the protein encoded by this gene binds caveolin-3, The protein encoded by this gene belongs to the ferlin family and is a skeletal muscle protein found associated with the sarcolemma |
| Purification method: |
This antibody was purified via Protein A |
| Storage conditions: |
50% glycerol and 0, Store refrigerated at 2 to 8 degrees Celcius for up to 1 year, 09% sodium azide, Keep the antibody in an aqueous buffered solution containing 1% BSA |
| Excitation Emission: |
512, 550nm/570, 615nm |
| Synonyms: |
DYSF, DYSF_HUMAN, Dysferlin Dystrophy associated fer 1 like protein Fer 1 like protein 1, Dysferlin limb girdle muscular dystrophy 2B, Dysferlin limb girdle muscular dystrophy 2B autosomal recessive, Dystrophy associated fer 1 like 1, Dystrophy associated fer 1 like protein, Dystrophy associated fer1 like 1, Dystrophy associated fer1 like protein, FER1L1, FLJ00175, FLJ90168, Fer 1 like protein 1, Fer1 like protein 1, LGMD 2B, LGMD2B, Limb girdle muscular dystrophy 2B, Limb girdle muscular dystrophy 2B autosomal recessive , MM, Miyoshi myopathy, DMAT |
| Properties: |
1 of the Dysferlin Antibody, Conjugated can be used in flow cytometry but typically shows lower fluorescence intensity comparable to that of PE or APC, Cy3 antibodies are excited by the 488-nanometer wave of an argon laser and the 633-nanometer line of a helium-neon diode laser, This Bioss Primary Conjugated Antibodies antibody is well suited for fluorescent microscopy, C, C for long term storage and for short term at + 5°, If you buy Antibodies supplied by Bioss Primary Conjugated Antibodies they should be stored frozen at - 24° |
| Gene target: |
Dysferlin Conjugated |
| Short name: |
Conjugated, Dysferlin Antibody |
| Technique: |
antibodies against human proteins, antibodies for, antibody Conjugates, Antibody |
| Label: |
Cy3 |
| Alternative name: |
cyanine 3 coupled, Dysferlin (Antibody to) |
| Alternative technique: |
antibodies |